Date published: 2025-9-6

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Cytokeratin 5/8 抗体 (5F295): sc-70928

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说明书
  • Cytokeratin 5/8抗体(5F295)是小鼠单克隆IgG1 κ, 在1篇文献中引用,规格为200 µg/ml
  • 针对human肺癌细胞系MR21
  • 推荐用于 mouse, rat 和 human 来源的Cytokeratin 5/8 WB, IP, IF, IHC(P) 和 FCM检测; 可能与 Cytokeratin 18产生交联反应
  • 还可偶联藻红蛋白 以及 FITC 用于IF, IHC(P) 和 FCM
  • 看 pan-Cytokeratin (C11): sc-8018,可查看有标记的 Cytokeratin 5/8 抗体,包括AC, HRP, FITC, PE, Alexa Fluor® 488, 594, 647, 680 和 790
  • m-IgG Fc BP-HRP 是 Cytokeratin 5/8 抗体 (5F295) 在 WB and IHC(P) 应用中的首选二抗检测试剂。该试剂现与Cytokeratin 5/8 抗体 (5F295) 组合成套装提供。 (请参阅下面的订购信息)。

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関連項目

细胞角蛋白由一组不同的中间丝蛋白(IFP)组成,在角质化和非角质化上皮组织中成对表达。细胞角蛋白在分化和组织特化中起着关键作用,并起着维持上皮细胞整体结构完整性的作用。细胞角蛋白已被发现是组织分化的有用标记,可直接用于恶性肿瘤的表征。细胞角蛋白5在正常基底细胞中表达。细胞角蛋白5基因(KRT5)的突变已被证明会导致常染色体显性遗传病大疱性表皮松解症(EB)。细胞角蛋白8表达见于上皮和上皮源性肿瘤。细胞角蛋白10和13在一部分鳞状细胞癌中高度表达,而细胞角蛋白18在大多数腺癌和基底细胞癌中表达。

仅限研究使用。不适用于诊断和治疗用途。

订购信息

产品名称产品编号规格价格数量收藏夹

Cytokeratin 5/8 抗体 (5F295)

sc-70928
200 µg/ml
RMB2377.00

Cytokeratin 5/8 (5F295): m-IgG Fc BP-HRP 套装

sc-539323
200 µg Ab; 10 µg BP
RMB2662.00

Cytokeratin 5/8 抗体 (5F295) FITC

sc-70928 FITC
200 µg/ml
RMB2482.00

Cytokeratin 5/8 抗体 (5F295) PE

sc-70928 PE
200 µg/ml
RMB2580.00

What is the recommended starting dilution for Western blot for sc-70928: Cytokeratin 5/8 (5F295) monoclonal antibody?

Asked by: Germaine
The recommended starting dilution for Western blot is 1:100 with a dilution range of 1:100-1:1000. This information, along with other technical specifications, is available in the recommended protocol: https://www.scbt.com/scbt/resources/protocols/western-immuno-blotting
Answered by: Technical Support
Date published: 2017-03-22
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Rated 5 out of 5 by from Great WB data in HepG2 samplesGreat WB data in HepG2 samples. -SCBT QC
Date published: 2015-04-11
Rated 3 out of 5 by from Worked with human transfected lysate by WBWorked with human transfected lysate by WB -SCBT QC
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Rated 4 out of 5 by from Single strong band in MCF7 whole cell lysatesSingle strong band in MCF7 whole cell lysates. -SCBT QC
Date published: 2015-01-30
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Cytokeratin 5/8 抗体 (5F295) is rated 4.0 out of 5 by 3.
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