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Shanghai Genechem Ltd normal liver cell line chang liver
Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma <t>cell</t> lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and <t>Chang</t> <t>liver</t> cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.
Normal Liver Cell Line Chang Liver, supplied by Shanghai Genechem Ltd, 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/normal+liver+cell+line+chang+liver/normal+liver+cell+line+chang+liver/pmc07081114-86-11-19
Average 90 stars, based on 1 article reviews
normal liver cell line chang liver - by Bioz Stars, 2026-09
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Article Title: Increased KIF21B expression is a potential prognostic biomarker in hepatocellular carcinoma

Journal: World Journal of Gastrointestinal Oncology

doi: 10.4251/wjgo.v12.i3.276

Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma cell lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and Chang liver cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.
Figure Legend Snippet: Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma cell lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and Chang liver cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.

Techniques Used: Quantitative Proteomics, Expressing

Related Articles

Quantitative Proteomics:

Article Title: Increased KIF21B expression is a potential prognostic biomarker in hepatocellular carcinoma
Article Snippet: HCC cell lines Hep-G2, BEL7402, BEL-7404, and SMMC-7721 and the normal liver cell line Chang liver were purchased from Shanghai Genechem Co., Ltd. (Shanghai, China). .. B

Expressing:

Article Title: Increased KIF21B expression is a potential prognostic biomarker in hepatocellular carcinoma
Article Snippet: HCC cell lines Hep-G2, BEL7402, BEL-7404, and SMMC-7721 and the normal liver cell line Chang liver were purchased from Shanghai Genechem Co., Ltd. (Shanghai, China). .. B



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Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma <t>cell</t> lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and <t>Chang</t> <t>liver</t> cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.
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Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma <t>cell</t> lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and <t>Chang</t> <t>liver</t> cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.
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Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma <t>cell</t> lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and <t>Chang</t> <t>liver</t> cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.
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Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma <t>cell</t> lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and <t>Chang</t> <t>liver</t> cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.
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Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma <t>cell</t> lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and <t>Chang</t> <t>liver</t> cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.
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Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma <t>cell</t> lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and <t>Chang</t> <t>liver</t> cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.
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Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma cell lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and Chang liver cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.

Journal: World Journal of Gastrointestinal Oncology

Article Title: Increased KIF21B expression is a potential prognostic biomarker in hepatocellular carcinoma

doi: 10.4251/wjgo.v12.i3.276

Figure Lengend Snippet: Differential expression of KIF21B in The Cancer Genome Atlas database and hepatocellular carcinoma cell lines. A and B: Differential expression levels of KIF21B in 50 pairs of matched hepatocellular carcinoma and adjacent normal tissues from the The Cancer Genome Atlas database ( P < 0.01); C: KIF21B expression was examined in BEL-7404, BEL-7402, Hep-G2, SMMC-7721, and Chang liver cells. All the data were normalized to mRNA expression levels of human GAPDH using the 2 -ΔΔCT method. All the experiments were conducted in triplicate. Data were analyzed by ANOVA or t -test. The data are reported as the mean ± SD. P < 0.05 was considered significant, a P < 0.05, b P < 0.01.

Article Snippet: HCC cell lines Hep-G2, BEL7402, BEL-7404, and SMMC-7721 and the normal liver cell line Chang liver were purchased from Shanghai Genechem Co., Ltd. (Shanghai, China).

Techniques: Quantitative Proteomics, Expressing