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The protein encoded by KRT1 is a member of the keratin gene family. Additionally we are shipping KRT1 Kits (3) and many more products for this protein.
Showing 10 out of 81 products:
Human Monoclonal KRT1 Primary Antibody for IHC (fro), IHC (p) - ABIN93714
Moll, Franke, Schiller, Geiger, Krepler: The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells. in Cell 1983
Show all 3 references for ABIN93714
In our study, the missense mutation in the proband and his mother with epidermolytic ichthyosis (show LBR Antibodies) was a single amino acid difference in codon 478, which causes more serious skin manifestations
Complete structure of an epithelial keratin 1/keratin 10 (show KRT10 Antibodies) dimer has been presented.
These findings indicate that exogenous FABP4 (show FABP4 Antibodies) interacts with plasma membrane proteins, specifically CK1 (show CSNK1A1L Antibodies).
analysis of a heterozygous novel splice junction mutation in the 2B domain of KRT1 in a family with diffuse palmoplantar keratoderma
In ichthyosis (show LBR Antibodies) with confetti, a causal de novo KRT1 mutation had a C-terminal frameshift, replacing 22 C-terminal AAs (show FGD1 Antibodies) with an alternate 30-AA peptide. It distorted the IF network and mislocalized to the nucleus. Reversion occurred by mitotic recombination.
In HeLa cells transiently expressing C2GnT-M (show GCNT3 Antibodies)-GFP, knockdown of KRT1 does not affect Golgi morphology but leaves C2GnT-M (show GCNT3 Antibodies) outside of the Golgi, resulting in the formation of sialyl-T antigen.
Decreased levels of cytokeratin-1 is associated with breast cancer.
Hsp74 (show HSPA9 Antibodies), a potential bladder cancer marker, has direct interaction with keratin 1.
Case Report/Letter: specific mutation in 2B domain of KRT1 gives rise to mild phenotype of epidermolytic hyperkeratosis (show KRT10 Antibodies) mimicking ichthyosis (show LBR Antibodies) bullosa of Siemens.
study reports 2 related women of Colombian origin, affected by a severe ichthyosis (show LBR Antibodies) curth-macklin phenotype, who present a novel KRT1 mutation c.1577delG (p.Gly526Alafs*88)
The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the spinous and granular layers of the epidermis with family member KRT10 and mutations in these genes have been associated with bullous congenital ichthyosiform erythroderma. The type II cytokeratins are clustered in a region of chromosome 12q12-q13.
67 kDa cytokeratin
, cytokeratin 1
, epidermolytic hyperkeratosis 1
, hair alpha protein
, keratin, type II cytoskeletal 1
, type-II keratin Kb1