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The protein encoded by KRT13 is a member of the keratin gene family. 再加上，我们可以发Keratin 13 抗体 (171) 和 Keratin 13 蛋白 (11)和数多这个蛋白质的别的产品。
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this study reports that KRT13 plays a directive role in prostate cancer bone, brain, and soft tissue metastases
Keratin 13 gene is epigenetically suppressed during TGFB1 (显示 TGFB1 ELISA试剂盒)-induced epithelial-mesenchymal transition in a human keratinocyte cell line.
Four rare missense variants were identified (ACTBL2 (显示 ACTBL2 ELISA试剂盒) rs73757391 (5q11.2), BTD (显示 BTD ELISA试剂盒) rs200337373 (3p25.1), KRT13 rs150321809 (17q21.2) and MC2R (显示 MC2R ELISA试剂盒) rs104894658 (18p11.21)), but only MC2R (显示 MC2R ELISA试剂盒) rs104894668 had a large effect size (OR = 9.66).
KRT13 expression is associated with poor prognosis at multiple stages of disease progression
Loss of CK13 expression is associated with invasive oral squamous cell carcinoma.
Low KRT13 mRNA expression is associated with oral squamous cell carcinoma.
Decreased KRT13 was associated with Esophageal Squamous Cell Carcinoma.
Our data provide mechanistic insights into the epigenetic silencing of KRT13 genes in OSCC cells and might be useful for the development of diagnostic markers and novel therapeutic approaches against OSCCs.
The immunofluorescent staining pattern of Wnt1 (显示 WNT1 ELISA试剂盒) and CK7 (显示 KRT7 ELISA试剂盒) as well as Wnt1 (显示 WNT1 ELISA试剂盒) and CK13 was consistent with IHC results. Thus, in pleomorphic adenoma, Wnt (显示 WNT2 ELISA试剂盒) is involved in tumor cell differentiation of peripheral columnar cells forming solid nests
Immunoexpression of CK13 and CK17 (显示 KRT17 ELISA试剂盒) in light green-stained superficial cells was associated with more severe morphological atypia in tongue squamous cell carcinoma
denervation caused an increase of Keratin (Krt)13 expression around taste buds
K13 cooperates with Myc (显示 MYC ELISA试剂盒) to promote lymphoma through elevated NF-kappaB (显示 NFKB1 ELISA试剂盒).
The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This type I cytokeratin is paired with keratin 4 and expressed in the suprabasal layers of non-cornified stratified epithelia. Mutations in this gene and keratin 4 have been associated with the autosomal dominant disorder White Sponge Nevus. The type I cytokeratins are clustered in a region of chromosome 17q21.2. Alternative splicing of this gene results in multiple transcript variants\; however, not all variants have been described.
, cytokeratin 13
, keratin, type I cytoskeletal 13
, type I keratin KA13
, 47 kDa cytokeratin
, keratin complex 1, acidic, gene 13