trap-eze detection kit (oncor inc) Search Results


90
Oncor Inc trapeze assay kit
Trapeze Assay Kit, supplied by Oncor Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/trapeze assay kit/product/Oncor Inc
Average 90 stars, based on 1 article reviews
trapeze assay kit - by Bioz Stars, 2026-02
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Oncor Inc trapeze telomerase detection kit
hTERT‐immortalized cell lines show prolonged lifespan with activated <t>telomerase</t> function. (a) Growth curve of hTERT‐immortalized OSE lines (IOSE‐C9, C10, C21) and parental normal OSE cells (NOSE21R) in 180 days of culture. IOSE‐C9, C10 and C21 cells show stable population growth rates 30 days after subcloning. (b) Serum dependence and growth factor dependence analysis. After culturing the hTERT immortal line IOSE‐C21 in complete medium (A), serum‐free medium (B) and growth factor‐free medium (C) for 14 days, cells underwent population growth arrest in serum‐free medium, and slowed their expansion in growth factor‐free medium, but with a change to elongated morphology. Compared to cultures in complete medium, there were significant decreases of live cell populations in both serum and growth factor withdrawn cultures (P < 0.001). (c) TRAP assay show positive telomerase activity in all three immortal lines. 1: Positive control; 2: IOSE‐C21; 3: IOSE‐C9; the missing control band indicates the existence of PCR inhibitor in reaction mix. 4: IOSE‐C10; 5: NOSE21R (parental cells). The lowest two bands of each lane present the PCR endogenous control. Lanes 1–4 show the telomere ladder with 6 base pair (T2AG3) difference between each band, which is a positive indication of telomerase activity. (d) Telomere length assays showed relatively longer telomere length in the three immortal cell lines compared to the parental cells. 1: Telomere ‘high‐level’ control (supplied by the commercial kit); 2: Telomere ‘low‐level’ control (supplied by the commercial kit); 3: NOSE21R (parental cells); 4: IOSE‐C21 cells at passage 9; 5: IOSE‐C21 cells at passage 14; 6: IOSE‐C21 cells at passage 18; 7: IOSE‐C10 cells at passage 4; 8: IOSE‐C10 cells at passage 5; 9: IOSE‐C9 cells at passage 4; 10: IOSE‐C9 cells at passage 5.
Trapeze Telomerase Detection Kit, supplied by Oncor Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/trapeze telomerase detection kit/product/Oncor Inc
Average 90 stars, based on 1 article reviews
trapeze telomerase detection kit - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

90
Oncor Inc trap-eze oncor
hTERT‐immortalized cell lines show prolonged lifespan with activated <t>telomerase</t> function. (a) Growth curve of hTERT‐immortalized OSE lines (IOSE‐C9, C10, C21) and parental normal OSE cells (NOSE21R) in 180 days of culture. IOSE‐C9, C10 and C21 cells show stable population growth rates 30 days after subcloning. (b) Serum dependence and growth factor dependence analysis. After culturing the hTERT immortal line IOSE‐C21 in complete medium (A), serum‐free medium (B) and growth factor‐free medium (C) for 14 days, cells underwent population growth arrest in serum‐free medium, and slowed their expansion in growth factor‐free medium, but with a change to elongated morphology. Compared to cultures in complete medium, there were significant decreases of live cell populations in both serum and growth factor withdrawn cultures (P < 0.001). (c) TRAP assay show positive telomerase activity in all three immortal lines. 1: Positive control; 2: IOSE‐C21; 3: IOSE‐C9; the missing control band indicates the existence of PCR inhibitor in reaction mix. 4: IOSE‐C10; 5: NOSE21R (parental cells). The lowest two bands of each lane present the PCR endogenous control. Lanes 1–4 show the telomere ladder with 6 base pair (T2AG3) difference between each band, which is a positive indication of telomerase activity. (d) Telomere length assays showed relatively longer telomere length in the three immortal cell lines compared to the parental cells. 1: Telomere ‘high‐level’ control (supplied by the commercial kit); 2: Telomere ‘low‐level’ control (supplied by the commercial kit); 3: NOSE21R (parental cells); 4: IOSE‐C21 cells at passage 9; 5: IOSE‐C21 cells at passage 14; 6: IOSE‐C21 cells at passage 18; 7: IOSE‐C10 cells at passage 4; 8: IOSE‐C10 cells at passage 5; 9: IOSE‐C9 cells at passage 4; 10: IOSE‐C9 cells at passage 5.
Trap Eze Oncor, supplied by Oncor Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/trap-eze oncor/product/Oncor Inc
Average 90 stars, based on 1 article reviews
trap-eze oncor - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

90
Oncor Inc trapeze detection kit
hTERT‐immortalized cell lines show prolonged lifespan with activated <t>telomerase</t> function. (a) Growth curve of hTERT‐immortalized OSE lines (IOSE‐C9, C10, C21) and parental normal OSE cells (NOSE21R) in 180 days of culture. IOSE‐C9, C10 and C21 cells show stable population growth rates 30 days after subcloning. (b) Serum dependence and growth factor dependence analysis. After culturing the hTERT immortal line IOSE‐C21 in complete medium (A), serum‐free medium (B) and growth factor‐free medium (C) for 14 days, cells underwent population growth arrest in serum‐free medium, and slowed their expansion in growth factor‐free medium, but with a change to elongated morphology. Compared to cultures in complete medium, there were significant decreases of live cell populations in both serum and growth factor withdrawn cultures (P < 0.001). (c) TRAP assay show positive telomerase activity in all three immortal lines. 1: Positive control; 2: IOSE‐C21; 3: IOSE‐C9; the missing control band indicates the existence of PCR inhibitor in reaction mix. 4: IOSE‐C10; 5: NOSE21R (parental cells). The lowest two bands of each lane present the PCR endogenous control. Lanes 1–4 show the telomere ladder with 6 base pair (T2AG3) difference between each band, which is a positive indication of telomerase activity. (d) Telomere length assays showed relatively longer telomere length in the three immortal cell lines compared to the parental cells. 1: Telomere ‘high‐level’ control (supplied by the commercial kit); 2: Telomere ‘low‐level’ control (supplied by the commercial kit); 3: NOSE21R (parental cells); 4: IOSE‐C21 cells at passage 9; 5: IOSE‐C21 cells at passage 14; 6: IOSE‐C21 cells at passage 18; 7: IOSE‐C10 cells at passage 4; 8: IOSE‐C10 cells at passage 5; 9: IOSE‐C9 cells at passage 4; 10: IOSE‐C9 cells at passage 5.
Trapeze Detection Kit, supplied by Oncor Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/trapeze detection kit/product/Oncor Inc
Average 90 stars, based on 1 article reviews
trapeze detection kit - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

90
Oncor Inc trap-eze telomerase detection kit f67402
hTERT‐immortalized cell lines show prolonged lifespan with activated <t>telomerase</t> function. (a) Growth curve of hTERT‐immortalized OSE lines (IOSE‐C9, C10, C21) and parental normal OSE cells (NOSE21R) in 180 days of culture. IOSE‐C9, C10 and C21 cells show stable population growth rates 30 days after subcloning. (b) Serum dependence and growth factor dependence analysis. After culturing the hTERT immortal line IOSE‐C21 in complete medium (A), serum‐free medium (B) and growth factor‐free medium (C) for 14 days, cells underwent population growth arrest in serum‐free medium, and slowed their expansion in growth factor‐free medium, but with a change to elongated morphology. Compared to cultures in complete medium, there were significant decreases of live cell populations in both serum and growth factor withdrawn cultures (P < 0.001). (c) TRAP assay show positive telomerase activity in all three immortal lines. 1: Positive control; 2: IOSE‐C21; 3: IOSE‐C9; the missing control band indicates the existence of PCR inhibitor in reaction mix. 4: IOSE‐C10; 5: NOSE21R (parental cells). The lowest two bands of each lane present the PCR endogenous control. Lanes 1–4 show the telomere ladder with 6 base pair (T2AG3) difference between each band, which is a positive indication of telomerase activity. (d) Telomere length assays showed relatively longer telomere length in the three immortal cell lines compared to the parental cells. 1: Telomere ‘high‐level’ control (supplied by the commercial kit); 2: Telomere ‘low‐level’ control (supplied by the commercial kit); 3: NOSE21R (parental cells); 4: IOSE‐C21 cells at passage 9; 5: IOSE‐C21 cells at passage 14; 6: IOSE‐C21 cells at passage 18; 7: IOSE‐C10 cells at passage 4; 8: IOSE‐C10 cells at passage 5; 9: IOSE‐C9 cells at passage 4; 10: IOSE‐C9 cells at passage 5.
Trap Eze Telomerase Detection Kit F67402, supplied by Oncor Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/trap-eze telomerase detection kit f67402/product/Oncor Inc
Average 90 stars, based on 1 article reviews
trap-eze telomerase detection kit f67402 - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

90
Oncor Inc trapeze elisa kit
hTERT‐immortalized cell lines show prolonged lifespan with activated <t>telomerase</t> function. (a) Growth curve of hTERT‐immortalized OSE lines (IOSE‐C9, C10, C21) and parental normal OSE cells (NOSE21R) in 180 days of culture. IOSE‐C9, C10 and C21 cells show stable population growth rates 30 days after subcloning. (b) Serum dependence and growth factor dependence analysis. After culturing the hTERT immortal line IOSE‐C21 in complete medium (A), serum‐free medium (B) and growth factor‐free medium (C) for 14 days, cells underwent population growth arrest in serum‐free medium, and slowed their expansion in growth factor‐free medium, but with a change to elongated morphology. Compared to cultures in complete medium, there were significant decreases of live cell populations in both serum and growth factor withdrawn cultures (P < 0.001). (c) TRAP assay show positive telomerase activity in all three immortal lines. 1: Positive control; 2: IOSE‐C21; 3: IOSE‐C9; the missing control band indicates the existence of PCR inhibitor in reaction mix. 4: IOSE‐C10; 5: NOSE21R (parental cells). The lowest two bands of each lane present the PCR endogenous control. Lanes 1–4 show the telomere ladder with 6 base pair (T2AG3) difference between each band, which is a positive indication of telomerase activity. (d) Telomere length assays showed relatively longer telomere length in the three immortal cell lines compared to the parental cells. 1: Telomere ‘high‐level’ control (supplied by the commercial kit); 2: Telomere ‘low‐level’ control (supplied by the commercial kit); 3: NOSE21R (parental cells); 4: IOSE‐C21 cells at passage 9; 5: IOSE‐C21 cells at passage 14; 6: IOSE‐C21 cells at passage 18; 7: IOSE‐C10 cells at passage 4; 8: IOSE‐C10 cells at passage 5; 9: IOSE‐C9 cells at passage 4; 10: IOSE‐C9 cells at passage 5.
Trapeze Elisa Kit, supplied by Oncor Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/trapeze elisa kit/product/Oncor Inc
Average 90 stars, based on 1 article reviews
trapeze elisa kit - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

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hTERT‐immortalized cell lines show prolonged lifespan with activated telomerase function. (a) Growth curve of hTERT‐immortalized OSE lines (IOSE‐C9, C10, C21) and parental normal OSE cells (NOSE21R) in 180 days of culture. IOSE‐C9, C10 and C21 cells show stable population growth rates 30 days after subcloning. (b) Serum dependence and growth factor dependence analysis. After culturing the hTERT immortal line IOSE‐C21 in complete medium (A), serum‐free medium (B) and growth factor‐free medium (C) for 14 days, cells underwent population growth arrest in serum‐free medium, and slowed their expansion in growth factor‐free medium, but with a change to elongated morphology. Compared to cultures in complete medium, there were significant decreases of live cell populations in both serum and growth factor withdrawn cultures (P < 0.001). (c) TRAP assay show positive telomerase activity in all three immortal lines. 1: Positive control; 2: IOSE‐C21; 3: IOSE‐C9; the missing control band indicates the existence of PCR inhibitor in reaction mix. 4: IOSE‐C10; 5: NOSE21R (parental cells). The lowest two bands of each lane present the PCR endogenous control. Lanes 1–4 show the telomere ladder with 6 base pair (T2AG3) difference between each band, which is a positive indication of telomerase activity. (d) Telomere length assays showed relatively longer telomere length in the three immortal cell lines compared to the parental cells. 1: Telomere ‘high‐level’ control (supplied by the commercial kit); 2: Telomere ‘low‐level’ control (supplied by the commercial kit); 3: NOSE21R (parental cells); 4: IOSE‐C21 cells at passage 9; 5: IOSE‐C21 cells at passage 14; 6: IOSE‐C21 cells at passage 18; 7: IOSE‐C10 cells at passage 4; 8: IOSE‐C10 cells at passage 5; 9: IOSE‐C9 cells at passage 4; 10: IOSE‐C9 cells at passage 5.

Journal: Cell Proliferation

Article Title: Human ovarian surface epithelial cells immortalized with hTERT maintain functional pRb and p53 expression

doi: 10.1111/j.1365-2184.2007.00462.x

Figure Lengend Snippet: hTERT‐immortalized cell lines show prolonged lifespan with activated telomerase function. (a) Growth curve of hTERT‐immortalized OSE lines (IOSE‐C9, C10, C21) and parental normal OSE cells (NOSE21R) in 180 days of culture. IOSE‐C9, C10 and C21 cells show stable population growth rates 30 days after subcloning. (b) Serum dependence and growth factor dependence analysis. After culturing the hTERT immortal line IOSE‐C21 in complete medium (A), serum‐free medium (B) and growth factor‐free medium (C) for 14 days, cells underwent population growth arrest in serum‐free medium, and slowed their expansion in growth factor‐free medium, but with a change to elongated morphology. Compared to cultures in complete medium, there were significant decreases of live cell populations in both serum and growth factor withdrawn cultures (P < 0.001). (c) TRAP assay show positive telomerase activity in all three immortal lines. 1: Positive control; 2: IOSE‐C21; 3: IOSE‐C9; the missing control band indicates the existence of PCR inhibitor in reaction mix. 4: IOSE‐C10; 5: NOSE21R (parental cells). The lowest two bands of each lane present the PCR endogenous control. Lanes 1–4 show the telomere ladder with 6 base pair (T2AG3) difference between each band, which is a positive indication of telomerase activity. (d) Telomere length assays showed relatively longer telomere length in the three immortal cell lines compared to the parental cells. 1: Telomere ‘high‐level’ control (supplied by the commercial kit); 2: Telomere ‘low‐level’ control (supplied by the commercial kit); 3: NOSE21R (parental cells); 4: IOSE‐C21 cells at passage 9; 5: IOSE‐C21 cells at passage 14; 6: IOSE‐C21 cells at passage 18; 7: IOSE‐C10 cells at passage 4; 8: IOSE‐C10 cells at passage 5; 9: IOSE‐C9 cells at passage 4; 10: IOSE‐C9 cells at passage 5.

Article Snippet: Telomerase activity was measured using the TRAPeze telomerase detection kit (Oncor Inc., Gaithersburg, MD, USA), following the manufacturer's protocol, for the radioactive assay (TRAP assay, telomere repeat amplification protocol).

Techniques: Subcloning, TRAP Assay, Activity Assay, Positive Control, Control