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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 101 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
Human Polyclonal KRT1 Primary Antibody for IHC, IHC (p) - ABIN4303928
Ambatipudi, Bhosale, Heath, Pandey, Kumar, Kane, Patil, Maru, Desai, Watt, Mahimkar: Downregulation of keratin 76 expression during oral carcinogenesis of human, hamster and mouse. in PLoS ONE 2013
Show all 2 references for ABIN4303928
Chicken Monoclonal KRT1 Primary Antibody for ELISA, FACS - ABIN4303932
Franchini, Ottaviani: Immunoreactive POMC-derived peptides and cytokines in the chicken thymus and bursa of Fabricius microenvironments: age-related changes. in Journal of neuroendocrinology 1999
Human Polyclonal KRT1 Primary Antibody for ICC, IF - ABIN4303929
DiTommaso, Cottle, Pearson, Schlüter, Kaur, Humbert, Smyth: Keratin 76 is required for tight junction function and maintenance of the skin barrier. in PLoS genetics 2014
Case Report: post-zygotic mosaicism of KRT/1o mutations in epidermolytic Ichthyosis (show LBR Antibodies).
KRT1 played an important role of maintaining epithelial barrier and its down-regulation in intestinal tissue was correlated with the progression of inflammatory bowel disease.
Report genetic/clinical spectrum of KRT1 mutations in keratinopathic ichthyosis (show LBR Antibodies).
demonstrated the presence of a genetic cutaneous mosaicism. Both patients carry the KRT1 pI479T substitution, but in the palmoplantar areas of one of them, only the mutated allele is expressed (hemizygous). This leads to highlight a new type of cutaneous mosaic, the palmoplantar mosaicism
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.
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