primary 184 antibodies against cyclin d1 Search Results


primary antibodies against cyclin d1, flag tag or tubulin  (MBL Life science)
90
MBL Life science primary antibodies against cyclin d1, flag tag or tubulin
Expression levels of <t>both</t> <t>cyclin</t> D1 variants in paired HCC tissues. Total RNA were prepared from 45 paired HCC tissues and 11 normal liver tissues. The expression of both cyclin D1 variants was quantitated by qRT-PCR and normalized to CTBP1. Each sample was tested in triplicate in two separate experiments. a The comparison of cyclin D1a expression levels among the HCC tumor, adjacent nontumor and the normal liver tissues. ANOVA test was used to analyze the difference of cyclin D1a expression levels among these groups. b The expression of cyclin D1b was compared as in ( a ). c Ratio of cyclin D1b versus cyclin D1a was compared as in ( a ). d The difference between cyclin D1a and cyclin D1b expression in the HCC tissues, adjacent nontumor tissues or the normal liver tissues. ANOVA test was used to analyze the difference of cyclin D1 expression levels among these groups. e The expression of cyclin D1a protein in 14 paired HCC tissues was detected by Western blot assay. <t>Tubulin</t> was used as an internal loading control in each lane. T tumor tissue, NT nontumor tissue
Primary Antibodies Against Cyclin D1, Flag Tag Or Tubulin, supplied by MBL Life science, 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/product/primary+184+antibodies+against+cyclin+d1/pmc04644212-60-14-15?v=MBL+Life+science
Average 90 stars, based on 1 article reviews
primary antibodies against cyclin d1, flag tag or tubulin - by Bioz Stars, 2026-08
90/100 stars
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primary antibodies against cyclin d1  (USA Cycling Inc)
90
USA Cycling Inc primary antibodies against cyclin d1
Expression levels of <t>both</t> <t>cyclin</t> D1 variants in paired HCC tissues. Total RNA were prepared from 45 paired HCC tissues and 11 normal liver tissues. The expression of both cyclin D1 variants was quantitated by qRT-PCR and normalized to CTBP1. Each sample was tested in triplicate in two separate experiments. a The comparison of cyclin D1a expression levels among the HCC tumor, adjacent nontumor and the normal liver tissues. ANOVA test was used to analyze the difference of cyclin D1a expression levels among these groups. b The expression of cyclin D1b was compared as in ( a ). c Ratio of cyclin D1b versus cyclin D1a was compared as in ( a ). d The difference between cyclin D1a and cyclin D1b expression in the HCC tissues, adjacent nontumor tissues or the normal liver tissues. ANOVA test was used to analyze the difference of cyclin D1 expression levels among these groups. e The expression of cyclin D1a protein in 14 paired HCC tissues was detected by Western blot assay. <t>Tubulin</t> was used as an internal loading control in each lane. T tumor tissue, NT nontumor tissue
Primary Antibodies Against Cyclin D1, supplied by USA Cycling 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/product/primary+184+antibodies+against+cyclin+d1/pm24129747-71-19-37?v=USA+Cycling+Inc
Average 90 stars, based on 1 article reviews
primary antibodies against cyclin d1 - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

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Expression levels of both cyclin D1 variants in paired HCC tissues. Total RNA were prepared from 45 paired HCC tissues and 11 normal liver tissues. The expression of both cyclin D1 variants was quantitated by qRT-PCR and normalized to CTBP1. Each sample was tested in triplicate in two separate experiments. a The comparison of cyclin D1a expression levels among the HCC tumor, adjacent nontumor and the normal liver tissues. ANOVA test was used to analyze the difference of cyclin D1a expression levels among these groups. b The expression of cyclin D1b was compared as in ( a ). c Ratio of cyclin D1b versus cyclin D1a was compared as in ( a ). d The difference between cyclin D1a and cyclin D1b expression in the HCC tissues, adjacent nontumor tissues or the normal liver tissues. ANOVA test was used to analyze the difference of cyclin D1 expression levels among these groups. e The expression of cyclin D1a protein in 14 paired HCC tissues was detected by Western blot assay. Tubulin was used as an internal loading control in each lane. T tumor tissue, NT nontumor tissue

Journal: Tumour Biology

Article Title: Influence of CCND1 G870A polymorphism on the risk of HBV-related HCC and cyclin D1 splicing variant expression in Chinese population

doi: 10.1007/s13277-015-3401-7

Figure Lengend Snippet: Expression levels of both cyclin D1 variants in paired HCC tissues. Total RNA were prepared from 45 paired HCC tissues and 11 normal liver tissues. The expression of both cyclin D1 variants was quantitated by qRT-PCR and normalized to CTBP1. Each sample was tested in triplicate in two separate experiments. a The comparison of cyclin D1a expression levels among the HCC tumor, adjacent nontumor and the normal liver tissues. ANOVA test was used to analyze the difference of cyclin D1a expression levels among these groups. b The expression of cyclin D1b was compared as in ( a ). c Ratio of cyclin D1b versus cyclin D1a was compared as in ( a ). d The difference between cyclin D1a and cyclin D1b expression in the HCC tissues, adjacent nontumor tissues or the normal liver tissues. ANOVA test was used to analyze the difference of cyclin D1 expression levels among these groups. e The expression of cyclin D1a protein in 14 paired HCC tissues was detected by Western blot assay. Tubulin was used as an internal loading control in each lane. T tumor tissue, NT nontumor tissue

Article Snippet: After blocking, membranes were incubated with primary antibodies against cyclin D1, Flag tag or tubulin (MBL, Aichi, Japan), overnight at 4 °C and then with the secondary antibodies conjugated with Cy5.5 (Buckinghamshire, UK) for 2 h in room temperature.

Techniques: Expressing, Quantitative RT-PCR, Comparison, Western Blot, Control