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The protein encoded by KRT13 is a member of the keratin gene family.
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Human Monoclonal KRT13 Primary Antibody pour IHC (fro), IHC - ABIN335223
Kopan, Traska, Fuchs: Retinoids as important regulators of terminal differentiation: examining keratin expression in individual epidermal cells at various stages of keratinization. dans The Journal of cell biology 1987
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Human Monoclonal KRT13 Primary Antibody pour IHC (fro), IHC - ABIN335339
Bauwens, De Groot, Ramaekers, Veldman, Huizing: Expression of intermediate filament proteins in the adult human vestibular labyrinth. dans The Annals of otology, rhinology, and laryngology 1992
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Mouse (Murine) Monoclonal KRT13 Primary Antibody pour IHC (p), WB - ABIN108618
Dhouailly, Xu, Manabe, Schermer, Sun et al.: Expression of hair-related keratins in a soft epithelium: subpopulations of human and mouse dorsal tongue keratinocytes express keratin markers for hair-, skin- and esophageal-types of ... dans Experimental cell research 1989
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Human Monoclonal KRT13 Primary Antibody pour IHC (fro), IHC (p) - ABIN335313
Dallenbach-Hellweg, Lang: Immunohistochemical studies on uterine tumors. I. Invasive squamous cell carcinomas of the cervix and their precursors. dans Pathology, research and practice 1991
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Human Polyclonal KRT13 Primary Antibody pour IHC (p), IHC - ABIN449543
Sajjan, Xie, Lefebre, Valvano, Forstner: Identification and molecular analysis of cable pilus biosynthesis genes in Burkholderia cepacia. dans Microbiology (Reading, England) 2003
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Human Monoclonal KRT13 Primary Antibody pour FACS, ELISA - ABIN969578
Jacques, Pereira, Maia, Cuzzi, Ramos-e-Silva: Expression of cytokeratins 10, 13, 14 and 19 in oral lichen planus. dans Journal of oral science 2009
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 (Montrer TGFB1 Anticorps)-induced epithelial-mesenchymal transition in a human keratinocyte cell line.
Four rare missense variants were identified (ACTBL2 (Montrer ACTBL2 Anticorps) rs73757391 (5q11.2), BTD (Montrer BTD Anticorps) rs200337373 (3p25.1), KRT13 rs150321809 (17q21.2) and MC2R (Montrer MC2R Anticorps) rs104894658 (18p11.21)), but only MC2R (Montrer MC2R Anticorps) 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 (Montrer WNT1 Anticorps) and CK7 (Montrer KRT7 Anticorps) as well as Wnt1 (Montrer WNT1 Anticorps) and CK13 was consistent with IHC results. Thus, in pleomorphic adenoma, Wnt (Montrer WNT2 Anticorps) is involved in tumor cell differentiation of peripheral columnar cells forming solid nests
Immunoexpression of CK13 and CK17 (Montrer KRT17 Anticorps) 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 (Montrer MYC Anticorps) to promote lymphoma through elevated NF-kappaB (Montrer NFKB1 Anticorps).
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