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"Kromosom merupakan substansi genetik pada makhluk hidup yang diwariskan ke generasi selanjutnya. Kromosom terbentuk melalui proses kondensasi selama siklus sel. Faktor-faktor yang mempengaruhi kondensasi kromosom adalah protein scaffold dan kation divalen, terutama ion kalsium (Ca2+). Peran ion kalsium terhadap kromosom masih terbatas pada kromosom manusia dan belum pernah dilaporkan pada kromosom tumbuhan. Tujuan penelitian ini untuk mengetahui peran ion kalsium terhadap struktur kromosom barley menggunakan mikroskop fluoresens dan scanning electron microscope. Kromosom barley diisolasi kemudian diberi perlakuan 1 mM BAPTA sebagai agen pengikat ion kalsium dan PBS sebagai kontrol. Terdapat perbedaan panjang dan struktur kromosom barley setelah diberikan perlakuan 1 mM BAPTA dibandingkan dengan kromosom kontrol. Kromosom kontrol memiliki panjang rata-rata 5,3 μm dengan struktur kromosom yang padat, sedangkan kromosom dengan perlakuan BAPTA memiliki panjang rata-rata 10,7 μm dengan struktur kromosom lebih renggang dan kurang padat. Hasil tersebut menunjukkan bahwa ion kalsium memiliki peranan penting dalam menjaga struktur kromosom barley.

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Chromosomes are genetic substances in living organisms that are passed on to the next generation. Chromosomes are formed through the process of condensation during the cell cycle. Factors that influence chromosome condensation are scaffold proteins and divalent cations, especially calcium ions (Ca2+). The role of calcium ions on chromosomes is still limited to human chromosomes and has never been reported on plant chromosomes. The purpose of this study was to determine the role of calcium ions on the structure of barley chromosomes using a fluorescence microscope and scanning electron microscope. The barley chromosome was isolated and then treated with 1 mM BAPTA as a calcium ion chelating agent and PBS as a control. According to the data obtained, there are differences in length and structure of barley chromosomes after being treated with 1 mM BAPTA compared to control chromosomes. The control chromosome has an average length of 5.3 μm with a compact chromosome structure and chromosomes with BAPTA treatment have an average length of 10.7 μm with a less condense chromosome structure. These results indicated that calcium ions have an important role on maintaining the structure of barley chromosomes."

"Kondensasi kromosom pada tahap metafase memiliki peranan penting dalam keberlangsungan siklus sel. Sejauh ini masih terus dilakukan penelitian mengenai faktor yang mempengaruhi kondensasi kromosom. Kation divalen, terutama kalsium (Ca2+) diketahui memiliki peranan penting dalam kondensasi kromosom manusia. Akan tetapi, peranan Ca2+ terhadap kromosom tumbuhan belum diketahui. Gandum merupakan salah satu organisme model dalam sitogenetika. Oleh karena itu, diperlukan penelitian mengenai efek Ca2+ kalsium terhadap kondensasi kromsosom gandum (Triticum spp.). Tujuan dari penelitian ini adalah untuk mengetahui pengaruh pemberian 1 mM BAPTA (1, 2-bis(2-aminophenoxy) ethane-N, N, N′, N′-tetraacetic acid), 1 mM EDTA (Ethylenediaminetetraacetic acid), sebagai pelekat Ca2+, terhadap struktur kromosom gandum menggunakan mikroskop cahaya dan Scanning Electron Microscope (SEM). Kecambah gandum dipotong bagian ujung akar dan diinkubasi di dalam larutan PFA (Paraformaldehyde) 2%. Sampel diinkubasi dengan enzim selulase 2,5 % dan pectoliase 2,5%. Setelah itu sampel diberi perlakuan masing-masing dengan 1 mM BAPTA, 1 mM EDTA, dan kontrol dengan PBS. Kromosom kemudian diwarnai dengan aceto orcein sedangkan yang diamati SEM dipreparasi melalui tahap fiksasi, post-fiksasi, staining, dehidrasi, dan dikeringkan dengan HMDS (hexamethyldisilazane) sebelum diamati menggunakan SEM. Hasil yang diperoleh pada pengamatan kuantitatif menunjukkan panjang rata-rata untuk kromosom kontrol 12,5±3,4 µm sedangkan pada perlakuan 1 mM BAPTA dan 1 mM EDTA panjang rata-rata yang diperoleh adalah 17,7±6,6 µm dan 41,9±16,3 µm. Struktur kromosom kontrol secara kualitatif lebih padat dan lebih terkondensasi. Akan tetapi kromosom yang diberi perlakuan 1 mM BAPTA dan 1 mM EDTA menunjukkan hasil yang lebih panjang, tersebar, dan terjadi dekondensasi kromosom sehingga serat-serat kromatin lebih terlihat jelas. Hal tersebut menunjukkan Ca2+ memiliki peranan penting dalam kondensasi kromosom gandum.

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Chromosome condensation at metaphase has an important role in the continuation of the cell cycle. Researches on the investigation of the major factors affecting chromosome condensation has been conducted so far. Divalent cations, especially Ca2+ has been reported to have an important role in human chromosome condensation. Nevertheless, its effect on the plant chromosome has yet to be evaluated. Wheat (Triticum spp.) is one of the model organisms in cytogenetics.Therefore, study to evaluate the effect of Ca2+ on wheat chromsosomes is required. The purpose of this study was to determine the effect of 1 mM BAPTA and 1 mM EDTA as the Ca2+ chelating agent on the wheat chromosomes using light microscope and SEM (Scanning Electron Microscope). The root tips of wheat sprouts was cut off and incubated in a 2% PFA (Paraformaldehyde)  solution. The sample was incubated with 2.5% cellulase and 2.5% pectoliase enzyme. After that, the samples were treated with 1 mM BAPTA, 1 mM EDTA, and PBS as control. Chromosome were then stained with aceto orcein, while sample for SEM were subjected to SEM preparation including fixation, post-fixtaion, staining, dehydration, and HMDS (hexamethyldisilazane)  drying. The results showed that the average length of the control chromosome was 12.5±3.4 µm, while those treated with 1 mM BAPTA and 1 mM EDTA showed the average length of 17.7 ± 6.6 µm and 41. 9 ± 16.3 µm, respectively. The qualitative observation of the control chromosomes showed the more compact and condensed structure. However, chromosomes treated with 1 mM BAPTA and 1 mM EDTA showed a longer, dispered, and decondensed chromosome showing the chromatin fibers. This result indicated that Ca2+ play an important role in wheat chromosome condensation."

"Kromosom memiliki peranan penting dalam menyimpan materi genetik setiap makhluk hidup. Salah satu faktor yang memengaruhi struktur kromosom adalah kation divalen termasuk ion tembaga (Cu2+). Hingga saat ini, belum terdapat penelitian yang menganalisis pengaruh Cu2+ terhadap struktur kromosom tumbuhan. Tumbuhan gandum (Triticum aestivum) merupakan organisme model terkait studi kromosom. Tujuan penelitian ini adalah mengetahui pengaruh Cu2+ pada berbagai konsentrasi (0, 20, 40, 80, 160, dan 1000 µM) terhadap struktur kromosom gandum menggunakan mikroskop cahaya dan scanning electron microscope (SEM). Biji gandum direndam di larutan Cu2+ selama 4 jam, kemudian dikecambahkan selama 48 jam. Ujung akar gandum kemudian disinkronisasi dengan kolkisin 0,01% dan difiksasi dengan larutan Carnoy. Sampel yang akan diamati menggunakan mikroskop cahaya kemudian dihidrolisis dengan HCl 1N, diwarnai dengan aceto-orcein, dan diamati di bawah mikroskop. Sampel yang akan diamati menggunakan SEM diberi enzim 2,5% selulase-pektinase, difiksasi menggunakan 2,5% glutaraldehid, post-fiksasi menggunakan OsO4, dehidrasi dengan etanol, dikeringkan dengan HMDS, dan diamati di bawah SEM. Hasil kualitatif menunjukkan struktur kromosom mulai dari yang paling terkondensasi hingga tidak terkondensasi berturut-turut adalah 20, 80, 40, 1000, 160, dan 0 µM Cu2+. Hasil kuantitatif menunjukkan panjang+lebar kromosom dari setiap perlakuan 0, 20, 40, 80, 160, dan 1000 µM Cu2+ berturut-turut adalah 18,378+1,676 µm, 11,484+2,028 µm, 16,035+1,765 µm, 15,402+1,791 µm, 17,427+1,550 µm, dan 16,321+1,500 µm. Uji perbandingan Tukey dan Dunn menunjukkan bahwa konsentrasi Cu2+ memberi pengaruh yang signifikan terhadap panjang dan lebar kromosom, khususnya pada konsentrasi 20 µM. Hasil dari penelitian ini menyatakan bahwa Cu2+ memiliki peran penting dalam menjaga struktur kromosom gandum.

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Chromosomes have an important role in storing the genetic material of every living creature. One of various factors that can affect the structure of chromosomes is divalent cations including copper ions (Cu2+). Until now, no research has analysed the effect of Cu2+ on plant chromosome structure. Wheat plants (Triticum aestivum) are a model organisms related to the study of chromosomes. This study aimed to determine the effect of Cu2+ at various concentrations (0, 20, 40, 80, 160, and 1000 µM) on wheat chromosome structure using a light microscope and scanning electron microscope (SEM). Wheat seeds were soaked in each Cu2+ solution for 4 hours and germinated for 48 hours. Root tips were then synchronized in colchicine 0.01% and fixed with Carnoy’s solution. For light microscope observation, the root tips were hydrolysed with 1N HCl, stained with aceto-orcein, and observed under the microscope. For SEM observation, the root tips were then treated with 2,5% cellulase-pectinase enzyme, fixed using glutaraldehyde, post-fixed using OsO4, dehydration using ethanol, dried with HMDS, and observed under SEM. The qualitative results showed that the chromosomes structure from most condensed to less condensed were 20, 80, 40, 1000, 160, and 0 µM Cu2+ respectively. The quantitative results showed that the length+width of the chromosomes from each treatment of 0, 20, 40, 80, 160, and 1000 µM Cu2+ were 18,378+1,676 µm, 11,484+2,028 µm, 16,035+1,765 µm, 15,402+1,791 µm, 17,427+1,550 µm, and 16,321+1,500 µm respectively. Tukey and Dunn comparison test showed that the concentration of Cu2+ significantly affected the length and width of chromosomes, especially at 20 µM concentration. The result of our study indicates that Cu2+ has an important role in maintaining the structure of wheat chromosomes.

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"Kondensasi kromosom memainkan peran penting dalam pembelahan mitosis. Ion Ca2+ diketahui berperan penting dalam proses kondensasi kromosom. Sejauh ini, studi tentang peran Ca2+ dalam kromosom sel hewan telah dilaporkan melalui penggunaan 1,2-bis (2- aminophenoxyethane-N,N,N′,N-tetraacetic acid) (BAPTA) dan Ethylenediamine- tetraacetic acid (EDTA) sebagai agen pengkelat ion Ca2+. Namun, penelitian tentang peran Ca2+ pada kromosom tanaman masih sangat terbatas. Penelitian ini dilakukan untuk mengetahui pengaruh Ca2+ terhadap kromosom gandum (Triticum aestivum) dengan pemberian 1mM BAPTA sebagai agen pengkelat ion Ca2+, 1mM EDTA sebagai agen pengkelat kation divalen umum, dan phosphate buffered saline (PBS) sebagai kontrol menggunakan mikroskop cahaya. Preparasi kromosom dilakukan dengan cara akar gandum dipotong dan diberi perlakuan colchicine sebelum dilarutkan dalam 2% Paraformaldehyde (PFA). Kemudian diinkubasi dengan 2,5% selulase dan 2,5% enzim pectoliase pada suhu 37°C selama 1 jam. Sampel kemudian disaring dan disentrifugasi untuk memperoleh sampel yang mengandung kromosom. Sampel kemudian diberi perlakuan dengan 1 mM BAPTA, 1 mM EDTA, dan PBS, dan diwarnai dengan Aceto orcein. Kromosom kemudian diamati di bawah mikroskop cahaya. Struktur dan kepadatan warna kromosom, serta panjang, lebar dan luas kromosom diamati dan diukur. Hasil pengamatan kualitatif menunjukkan bahwa struktur kromosom pada kontrol lebih rapat dan pendek sedangkan kromosom yang diberi perlakuan 1 mM BAPTA dan 1 mM EDTA mengalami dekondensasi, melebar, dan berwarna pucat. Hasil pengukuran kuantitatif menunjukkan bahwa kromosom Kontrol, BAPTA, dan EDTA masing-masing memiliki panjang 10.763 m, 14.845 m, 17.154 m, lebar 1.570 m, 1.637 m, 1.723 m, dan luas 18.172 m, 24.644 m, 29.687 M. Hasil uji statistik menunjukkan bahwa pengaruh BAPTA dan EDTA terhadap panjang dan luas kromosom berbeda nyata (α < 0,05). Hal ini membuktikan bahwa Ca2+ memiliki peran penting dalam menjaga struktur kromosom gandum.

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Chromosomal condensation plays an important role in the mitotic division. Ca2+ ions are known to play an important role in the chromosome condensation process. So far, studies on the role of Ca2+ in animal cell chromosomes have been reported using 1,2-bis (2-amino phenoxy ethane N, N, N′, N-tetraacetic acid) (BAPTA) and Ethylene diamine tetraacetic acid (EDTA) as Ca2+ ions chelating agents. However, research on the role of Ca2+ on plant chromosomes is still very limited. This study was conducted to determine the effect of Ca2+ on wheat chromosomes (Triticum aestivum) by administering 1mM BAPTA as a Ca2+ ion chelating agent, 1 mM EDTA as a general divalent cation chelating agent, and phosphate-buffered saline (PBS) as a control using a light microscope. For chromosome preparation, the root tips of wheat were cut and pretreated with colchicine before being dissolved in 2% Paraformaldehyde (PFA). The roots were then incubated with 2.5% cellulase and 2.5% pectoliase enzyme at 37°C for 1hour. The sample is then filtered and centrifuged to obtain a sample containing chromosomes. Samples were then treated with 1 mM BAPTA, 1 mM EDTA, and PBS and stained with Aceto orcein. Chromosomes were then observed under a light microscope. The structure and color density of the chromosomes were observed. The length, width, and area of the chromosomes were also measured. The qualitative observations showed that the chromosome structure in control was denser and shorter while the chromosomes treated with 1 mM BAPTA and 1 mM EDTA were decondensed, widened, and had pale color. The quantitative measurement showed that length, width, and area of chromosomes for in control, BAPTA, and EDTA were 10.763 m, 14.845 m, 17.154 m; 1.570 m, 1.637 m, 1.723 m; and 18.172 m, 24.644 m, 29.687 M respectively. The statistical results showed that the effect of BAPTA and EDTA on the length and area of chromosomes were significantly different (α < 0.05). This result proves that Ca2+ has a vital role in maintaining the chromosomal structure of wheat."

"Kromosom merupakan untai DNA yang mengalami penebalan akibat kondensasi. Kondensasi struktur kromosom sangat mempengaruhi segregasi kromosom saat fase mitotik. Penelitian sebelumnya telah melaporkan bahwa kondensasi kromosom sel HeLa dipengaruhi oleh ion kalsium (Ca2+), namun pengaruh Ca2+ pada kromosom manusia normal belum diketahui. Penelitian ini bertujuan untuk mengetahui pengaruh terhadap struktur kromosom limfosit manusia dengan pemberian 1 mM 1, 2-bis(2-aminophenoxy)ethane-N-N,N’,N’-tetraacetic acid (BAPTA, chelator Ca2+), 1 mM ethylenediaminetetraacetic acid (EDTA, chelator kation), dan PBS (kontrol) yang diamati menggunakan mikroskop cahaya. Sampel darah dikultur selama 72 jam, kemudian kromosom limfosit diisolasi dan diberi perlakuan 1 mM BAPTA, 1 mM EDTA, dan PBS. Kromosom diwarnai dengan Giemsa dan diamati dengan mikroskop cahaya. Hasil yang diperoleh menunjukkan struktur kromosom kontrol lebih pendek, padat, serta memiliki intensitas pewarna yang pekat dibandingkan dengan kromosom yang diberi perlakuan 1 mM BAPTA dan 1 mM EDTA yang memiliki struktur yang lebih panjang, lebih berongga, serta intensitas pewarna yang kurang pekat. Hasil analisis kuantitatif menunjukkan panjang, lebar, dan luas rata-rata kromosom kontrol sebesar 1,73±0,73 μm, 0,55±0,43 μm, dan 3,5±2,17 μm2, sedangkan panjang, lebar, dan luas rata-rata kromosom yang diberi 1 mM BAPTA sebesar 2,91±1,3 μm, 1,43±0,43 μm, dan 4,17±2,75 μm2. Rata-rata panjang dan lebar kromosom yang diberi 1 mM EDTA sebesar 2,26±0,52 μm dan 0,93±0,29 μm. Hasil tersebut memperlihatkan bahwa Ca2+ berperan penting dalam kondensasi struktur kromosom limfosit.

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The Chromosome is a DNA strand that undergoes thickening due to condensation. Condensation of chromosomal structure affects the segregation of chromosomes during the mitotic phase. Previous studies have reported that chromosomal condensation of HeLa cells is affected by calcium ions (Ca2+). Nevertheless, the effect of Ca2+ on human normal cells has yet to be investigated. This study aims to determine the effect of Ca2+ on the chromosomal structure of human lymphocyte by the treatments of 1 mM 2-bis(2-aminophenoxy)ethane-N-N,N’,N’-tetraacetic acid (BAPTA, a Ca2+ chelator), 1 mM ethylenediaminetetraacetic acid (EDTA, a cation chelator), and PBS (control), using a light microscope. The blood sample was cultured for 72 hours, followed by lymphocyte chromosomes isolation. After that, the samples were treated with PBS (control), 1 mM BAPTA, and 1 mM EDTA. Chromosomes were then stained with Giemsa and observed using a light microscope. The qualitative analysis showed that control chromosomes have shorter, and more condensed structures with a high dye intensity compared with those treated with 1 mM BAPTA and 1 mM EDTA which showed a longer and fibrous structure with low dye intensity. The quantitative analysis showed that the average length, width, and area of the control chromosome was 1.73±0.73 μm, 0.55±0.2 μm, and 3.5±2.17 μm2, respectively. while those treated with 1 mM BAPTA were 2.91±1.3 μm, 1.43±0.43 μm, and 4.17±2.75 μm2. Then, the average length and width of 1 mM EDTA chromosome was 2.26±0.52 μm and 0.93±0.29 μm. These results showed that Ca2+ plays an important role in the lymphocyte chromosome structure."

"[ABSTRAKLatar Belakang: Peran root surface conditioning terhadap keberadaan smear layer.Tujuan: Menganalisis hubungan antara penggunaan root surface conditioning (minosiklin 2,1% dan EDTA 24%) terhadap keberadaan smear layer setelah penghalusan akar gigi. Metoda: Sepuluh gigi manusia yang dicabut akibat kelainan periodontal dan dilakukan penghalusan akar. Gigi dipotong pada daerahsepertiga servikal, dan 30 spesimen yang terbentuk dibagi dalam tiga kelompok.Hasil: Tidak ada perbedaan signifikan terhadap tingkat keberadaan smear layer antara kelompok minosiklin maupun EDTA (p=0,759). Terdapat perbedaan signifikan antara kelompok minosiklin dan EDTA dengan salin sebagai kontrol (p=0,00). Kesimpulan: Ada hubungan antara penggunaan root surface conditioning terhadap keberadaan smear layer.

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ABSTRACTBackground: Role of root surface conditioning of the existence of smear layer.Objective: To analyze the smear layer on root surface conditioned withminocycline HCl 2,1% , EDTA gel 24%, after root planed.Materials and methods: Ten human teeth removed due to chronic periodontitis were collected and root planed. The teeth were sectioned on 1/3 cervikal, 30 specimens were divided into three groups. Results: No significant differences of smear layer between minocycline and EDTA (p=0,759). There was significant differences of minocycline and EDTA group compare to saline (p=0,00).Conclusion: There was relationship of root surface conditioning treatment with smear layer.;Background: Role of root surface conditioning of the existence of smear layer.Objective: To analyze the smear layer on root surface conditioned withminocycline HCl 2,1% , EDTA gel 24%, after root planed.Materials and methods: Ten human teeth removed due to chronic periodontitis were collected and root planed. The teeth were sectioned on 1/3 cervikal, 30 specimens were divided into three groups. Results: No significant differences of smear layer between minocycline and EDTA (p=0,759). There was significant differences of minocycline and EDTA group compare to saline (p=0,00).Conclusion: There was relationship of root surface conditioning treatment with smear layer., Background: Role of root surface conditioning of the existence of smear layer.Objective: To analyze the smear layer on root surface conditioned withminocycline HCl 2,1% , EDTA gel 24%, after root planed.Materials and methods: Ten human teeth removed due to chronic periodontitis were collected and root planed. The teeth were sectioned on 1/3 cervikal, 30 specimens were divided into three groups. Results: No significant differences of smear layer between minocycline and EDTA (p=0,759). There was significant differences of minocycline and EDTA group compare to saline (p=0,00).Conclusion: There was relationship of root surface conditioning treatment with smear layer.]"

"A nonconductor optical technique, having lateral resolution of about 5 μm and vertical resolution of about 0.09 μm, for surface profile (roughness) measurement was studied. It based on a heterodyne interferometer in which two orthogonal polarized beams of slightly different frequencies were used in a modified interference microscope. The beams scanned the surface of a work piece, and the reflected beams were allowed to interfere with one another. The phase of the beat frequency of the interfering return beams is directly proportional to the surface height. The result of a surface measurement include graphical displays of surface profile, roughness (Ra), root mean square (rms) and peak to valley (P-V) value."

"Kanker serviks menjadi kanker penyebab kematian tertinggi ketiga di Indonesia setelah kanker paru-paru dan payudara. Metode pencegahan seperti vaksin HPV dan metode pengobatan seperti pembedahan, kemoterapi, dan radioterapi telah dikembangkan. Akan tetapi, masih dibutuhkan pengembangan pengobatan alternatif, salah satunya adalah dari tumbuhan herbal dengan senyawa aktif citronellol. Penelitian-penelitian terdahulu membuktikan bahwa citronellol dapat menurunkan viabilitas dengan menginduksi apoptosis pada beberapa sel kanker, seperti sel kanker paru-paru, payudara, dan darah. Tujuan penelitian ini adalah untuk mengetahui pengaruh citronellol terhadap viabilitas sel HeLa menggunakan mikroskop fluoresens. Variasi konsentrasi 10, 25, 50, dan 100 µg/mL citronellol dengan waktu inkubasi 48 jam diujikan pada sel HeLa. Uji viabilitas dilakukan dengan uji WST-1 dan deteksi apoptosis dilakukan dengan pewarnaan Annexin V-FITC/PI menggunakan mikroskop fluoresens. Hasil uji dengan ANAVA satu arah menunjukkan tidak terdapat pengaruh signifikan dari citronellol terhadap viabilitas sel HeLa. Konsentrasi 10 µg/mL cenderung menurunkan viabilitas sel HeLa dibandingkan kontrol. Pengamatan dengan mikroskop fluoresens menunjukkan terdeteksinya sel apoptosis yang lebih tinggi dibandingkan dengan sel nekrosis dan perubahan morfologi pada sel late apoptosis. Penelitian lebih lanjut diperlukan untuk mengetahui lebih jauh pengaruh citronellol terhadap sel HeLa.

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Cervical cancer is the third leading cause of cancer death in Indonesia following lung cancer and breast cancer.  Prevention methods such as the HPV vaccine and treatment methods such as surgery, radiotherapy, and chemotherapy have been developed. However, the development of alternative medicine is still needed, one of which is from herbal plants with the active compound of citronellol. Previous studies have shown that citronellol can reduce viability by inducing apoptosis in some cancer cells, such as lung, breast, and blood cancer cells. This study aims to determine the effects of citronellol on HeLa cells viability and to detect apoptosis by Annexin V- FITC/PI staining using a fluorescence microscope. Concentration variations of 10, 25, 50, and 100 µg/mL citronellol with an incubation time of 48 hours were treated on HeLa cells. A viability test was carried out by WST-1 test and apoptosis detection was carried out by Annexin V-FITC/PI staining using a fluorescence microscope. The results of the one-way ANOVA test showed that there was no significant effect of different concentrations of citronellol on the viability of HeLa cells. The concentrations of 10 µg/mL of citronellol tended to decrease HeLa cells viability. Observations with fluorescence microscope showed a higher detection rate of apoptotic cells than necrotizing cells and a more visible morphological changes in late apoptotic cells. Furthermore, fluorescence microscopy detected apoptotic cells. Further study is required to get a more comprehensive information on the effects of citronellol on HeLa cells."

"Ion kalsium (Ca2+) adalah salah satu kation divalen yang berperan dalam proses kondensasi kromosom. Pengaruh Ca2+ pada kondensasi kromosom dengan melihat pola banding dan nilai kromosom belum diketahui. Penelitian ini bertujuan untuk mengetahui pengaruh ion kalsium (Ca2+) pada kondensasi struktur kromosom sel HeLa dengan teknik G-banding-trypsin-Leishman (GTL-banding) dan karyotyping. Sebaran kromosom pada tahap metafase diperoleh dengan mengkultur sel HeLa pada suhu 37 °C (5% CO2). BAPTA 1 mM sebagai chelator spesifik Ca2+ dan EDTA 1 mM sebagai chelator kation diberikan sebelum pemanenan kromosom. Kromosom yang telah dipanen selanjutnya dilakukan banding dengan pewarna Leishman. Pengaruh Ca2+ pada kondensasi kromosom diamati dengan membandingkan kromosom pada kelompok perlakuan dengan kelompok kontrol. Data dianalisis secara kualitatif dengan mengamati struktur kromosom dan pola banding kromosom, serta secara kuantitatif dengan mengacu pada Quality Assessment (QA) berdasarkan International System for Human Cytogenetics Nomenclature (ISCN). Hasil penelitian menunjukkan bahwa kromosom pada kelompok kontrol memiliki struktur yang padat dengan pola banding yang jelas teramati dengan nilai kromosom 2 hingga 5. Kelompok perlakuan 1 mM BAPTA memiliki struktur kromosom yang tidak padat dengan ukuran yang lebih besar dari kelompok kontrol dan memiliki pola banding yang kurang jelas dengan nilai kromosom 2 hingga 5. Kelompok perlakuan 1 mM EDTA memiliki struktur kromosom yang tidak padat dan fibrous dengan ukuran yang lebih besar dan panjang dari kelompok kontrol serta memiliki pola banding yang kurang jelas dengan nilai kromosom 2 hingga 6. Kromosom pada kelompok perlakuan 1 mM BAPTA dan 1 mM EDTA memiliki struktur lebih tidak padat dan pola banding yang kurang jelas jika dibandingkan dengan kelompok kontrol sehingga mengindikasikan peran Ca2+ dalam kondensasi struktur kromosom.

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Calcium ion (Ca2+) is one of the divalent cations involved in the chromosome condensation process. The effect of Ca2+ on chromosome condensation by observing banding patterns and chromosome value has yet known. This study aimed to determine the effect of calcium ion (Ca2+) on HeLa cell chromosome structure condensation using G-banding-Trypsin-Leishman (GTL-banding) technique and karyotyping. Metaphase chromosome spreads were obtained by culturing the HeLa cell at 37 ℃ (5% CO2). 1 mM BAPTA as Ca2+ chelator and 1 mM EDTA as cation chelator was added prior to the chromosome harvest. G-banding was carried out on harvested chromosomes using Leishman dye. The effect of Ca2+ on chromosome condensation was determined by comparing the treated chromosome to the control chromosome. The data were obtained and analyzed qualitatively by observing chromosome structure and banding pattern, as well as quantitatively by referring to the International System for Human Cytogenetics Nomenclature (ISCN). The result showed that the chromosome in the control group had a condensed structure with a clear banding pattern and chromosome value ranged from 2 to 5. Chromosome treated with 1 mM BAPTA had a less condensed structure with a bigger size compared to the control group and had chromosome value ranged from 2 to 5. Chromosome treated with 1 mM EDTA was also less condensed with longer and fibrous structure and had chromosome value ranged from 2 to 6. BAPTA-treated and EDTA-treated chromosomes had a less condensed structure with less clear banding pattern compared to the control which indicated the role of Ca2+ in the chromosome condensation process."

"Ion kalsium (Ca2+) merupakan kation yang berperan dalam kondensasi kromosom. Berbagai penelitian mengenai pengaruh Ca2+ terhadap struktur kromosom telah dilaporkan. Akan tetapi, penelitian-penelitian tersebut masih terbatas pada galur sel kanker atau sel hewan mamalia dengan pendekatan analisis ultrastruktur. Pengaruh Ca2+ terhadap struktur dan pola banding kromosom pada sel manusia non-kanker belum diketahui. Penelitian ini bertujuan untuk mengetahui pengaruh Ca2+ terhadap struktur dan pola banding kromosom dari sel darah manusia melalui teknik GTL-banding. Sel darah manusia dikultur, kemudian dilakukan pemanenan kromosom dan banding menggunakan pewarna Leishman. Pengaruh Ca2+ dievaluasi dengan menginkubasikan kromosom pada dua larutan berbeda, yaitu larutan 1 mM BAPTA sebagai chelator spesifik Ca2+ dan 1 mM EDTA sebagai chelator kation, dan dibandingkan dengan kontrol. Data yang diperoleh dianalisis secara kualitatif dengan mengamati struktur dan pola banding kromosom, serta secara kuantitatif dengan menentukan nilai kromosom berdasarkan kriteria Quality Assessment (QA) dari International System for Human Cytogenetics Nomenclature (ISCN). Hasil yang diperoleh menunjukkan kromosom kelompok perlakuan 1 mM BAPTA memiliki struktur tidak padat, membentuk struktur fibrous, dan berukuran lebih lebar dibandingkan kromosom kontrol dengan pola banding tidak jelas dan kabur. Kromosom kelompok perlakuan 1 mM EDTA membentuk struktur tidak padat dan berukuran lebih panjang dibandingkan kelompok kontrol. Rata-rata nilai kromosom pada kelompok kontrol, BAPTA, dan EDTA berturut-turut adalah 4,467 ± 0,78; 4,30 ± 0,75; dan 4,467 ± 0,86. Perbedaan struktur kromosom, pola banding, dan rata-rata nilai kromosom pada kromosom 1 mM BAPTA dan 1 mM EDTA menunjukkan bahwa kation Ca2+ merupakan faktor penting dalam kondensasi struktur kromosom.

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Calcium ion (Ca2+) is a cation that has a major role in chromosome condensation. Studies about Ca2+ effect in chromosome structure have been reported. However, the studies are limited for cancer cell lines using the ultrastructure analysis approach. The effect of Ca2+ on chromosome structure and banding pattern of the human non-cancer cell line is still unknown. This study aims to determine the effect of Ca2+ on human blood cell chromosome structure and banding pattern using the GTL-banding technique. The blood cell was cultured and then the chromosome was harvested and banded with Leishman dye. The Ca2+ effect was evaluated by using 1 mM BAPTA as Ca2+ specific chelator and 1 mM EDTA as common cation chelator and then compared with the control. The data were then analysis both qualitatively by observing chromosome structure and banding pattern, as well as quantitatively by determining chromosome value based on Quality Assessment (QA) from International System for Human Cytogenetics Nomenclature (ISCN). The result showed that the BAPTA-treated chromosome structure was fuzzy, fibrous, and wider than the control group with a less clear banding pattern than the control. In addition, EDTA-treated chromosome structure was less condensed and longer than those of the control. The mean chromosome value of control, BAPTA-, and EDTA-treated chromosome are 4.467 ± 0.78; 4.30 ± 0.75; and 4.467 ± 0.86. Distinct characteristic of chromosome structure, banding pattern, and mean of chromosome value from BAPTA- and EDTA-treated chromosome further indicates that Ca2+ plays an important role in chromosome condensation."