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KRT14 encodes a member of the keratin family, the most diverse group of intermediate filaments. Additionally we are shipping Keratin 14 Proteins (18) and Keratin 14 Kits (4) and many more products for this protein.
Showing 10 out of 297 products:
Human Monoclonal KRT14 Primary Antibody for FACS, IHC (fro) - ABIN118965
Lane, Alexander: Use of keratin antibodies in tumor diagnosis. in Seminars in cancer biology 1991
Show all 9 references for ABIN118965
Human Monoclonal KRT14 Primary Antibody for FACS, IF - ABIN118964
Purkis, Steel, Mackenzie, Nathrath, Leigh, Lane: Antibody markers of basal cells in complex epithelia. in Journal of cell science 1991
Show all 7 references for ABIN118964
Dog (Canine) Monoclonal KRT14 Primary Antibody for IHC (fro), FACS - ABIN1106908
Smedts, Ramaekers, Troyanovsky, Pruszczynski, Robben, Lane, Leigh, Plantema, Vooijs: Basal-cell keratins in cervical reserve cells and a comparison to their expression in cervical intraepithelial neoplasia. in The American journal of pathology 1992
Show all 7 references for ABIN1106908
Cow (Bovine) Polyclonal KRT14 Primary Antibody for IHC (fro), IHC (p) - ABIN113455
Herrmann, van der Hoeven, Grone, Stewart, Langbein, Kaiser, Liebisch, Gosch, Buchkremer, Drobnik, Schmitz, Stremmel: Mice with targeted disruption of the fatty acid transport protein 4 (Fatp 4, Slc27a4) gene show features of lethal restrictive dermopathy. in The Journal of cell biology 2003
Show all 6 references for ABIN113455
Cat (Feline) Monoclonal KRT14 Primary Antibody for IHC (fro), FACS - ABIN1106910
Ivanyi, Minke, Hageman, Groeneveld, van Doornewaard: Patterns of expression of feline cytokeratins in healthy epithelia and mammary carcinoma cells. in American journal of veterinary research 1992
Show all 2 references for ABIN1106910
Human Monoclonal KRT14 Primary Antibody for IHC (fro), IHC (p) - ABIN264414
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 2 references for ABIN264414
Human Monoclonal KRT14 Primary Antibody for FACS, IHC (p) - ABIN1687795
Kang, Kannan, Zhang, Martinez, Rosin, Eaves: Characterization of Epithelial Progenitors in Normal Human Palatine Tonsils and Their HPV16 E6/E7-Induced Perturbation. in Stem cell reports 2015
Human Polyclonal KRT14 Primary Antibody for EIA, WB - ABIN453159
Barcelos, Sotto: Comparative analysis of the expression of cytokeratins (1, 10, 14, 16, 4), involucrin, filaggrin and e-cadherin in plane warts and epidermodysplasia verruciformis plane wart-type lesions. in Journal of cutaneous pathology 2009
Cow (Bovine) Polyclonal KRT14 Primary Antibody for WB - ABIN2792304
Pfendner, Sadowski, Uitto: Epidermolysis bullosa simplex: recurrent and de novo mutations in the KRT5 and KRT14 genes, phenotype/genotype correlations, and implications for genetic counseling and prenatal diagnosis. in The Journal of investigative dermatology 2005
findings indicate that ouro1 and ouro2 participate in the process of tail regression as immune antigens and highlight the possibility that the acquired immune system contributes not only to self-defense but also to remodeling processes in morphogenesis.
identification of 29 different mutations in KRT5 (show KRT5 Antibodies) and KRT14, 11 of which were novel, in a Polish cohort of epidermolysis bullosa simplex patients
findings reveal K14 as a key regulator of metastasis and establish the concept that K14(+) epithelial tumor cell clusters disseminate collectively to colonize distant organs
all keratins tested, except for keratin 14, were evenly expressed in all trophoblast cells. Keratin 14 was expressed in a subset of CK7 (show KRT7 Antibodies) positive cells
report a family with a novel heterozygous missense mutation p.Leu418Gln in the KRT14 gene causing epidermolysis bullosa simplex with variable phenotype
investigated a family in which 1 of 3 children was diagnosed with a localized form of epidermolysis bullosa simplex and there was no family history of blistering; results argue against parental somatic and germline mosaicism in the family and suggest the novel p.Val270Ala mutation in KRT14 also represents a de novo event which occurred in the proband
KRT14 protein genetic mutation is a good indicator of disease progression in patient diagnosed with epidermolysis bullosa simplex.
Analysis of K14 variants with single or multiple substitutions of cysteine residues points to a spatial and temporal hierarchy in how Cys-4/Cys-40 and Cys-367 regulate keratin assembly in vitro and filament dynamics in live keratinocytes
in silico analysis of all epidermolysis bullosa simplex causing point mutations on the 2B domain of K5 and K14; result showed all pathogenic point mutations exert their dominant negative effect on the K5/K14 coiled-coil heterodimer complex by altering interchain interaction,leading to changes in stability and assembly competence of the heterodimer complex
The present study confirmed that CK14, but not CK20 (show KRT20 Antibodies) or CK7 (show KRT7 Antibodies), is expressed in urothelial carcinoma with squamous differentiation and squamous cell carcinoma of the urinary bladder.
plectin (show PLEC Antibodies) interacts with keratins 5 and 14 in a process associated with epidermolysis bullosa simplex
Disulfide bonding is a novel and important mechanism regulating the assembly, intracellular organization, and dynamics of K14-containing intermediate filaments in skin keratinocytes.
K14-VEGF transgenic mouse a valuable model to study novel immunotherapies for psoriasis
autoantibodies in Scurfy (show FOXP3 Antibodies) mice and patients with IPEX (show FOXP3 Antibodies) target keratin 14
nipple connective tissue and its development: insights from the keratin 14-PTHrP (show PTHLH Antibodies) mouse
The keratin-14 IL-4 (show IL4 Antibodies) transgenic (Tg) mouse model of atopic dermatitis (AD) is characterized by skin infiltration of T cells, early up-regulation of T(h)2 cytokines and late surge of T(h)1 cytokines.
These studies provide a potential mechanism by which deltaNp63 directly governs the expression of K14 in a keratinocyte-specific manner.
Study describes the expression profile of claudins and keratin markers in the accelerated epidermal permeability barrier formation of K14-CaSR (show CASR Antibodies) transgenic mice during development as compared to the wild type from E12.5 to newborn stages.
IL-6 (show IL6 Antibodies) and IFN-gamma (show IFNG Antibodies) stimulated VEGF-A (show VEGFA Antibodies) mRNA production in the skin and in primary keratinocytes of keratin 14 IL-4 (show IL4 Antibodies) transgenic mice
DeltaNp63 alone can restore the expression of the basal keratins and reinitiate the failed epidermal differentiation program in the skin of p63 (show CKAP4 Antibodies) null animals.
This gene encodes a member of the keratin family, the most diverse group of intermediate filaments. This gene product, a type I keratin, is usually found as a heterotetramer with two keratin 5 molecules, a type II keratin. Together they form the cytoskeleton of epithelial cells. Mutations in the genes for these keratins are associated with epidermolysis bullosa simplex. At least one pseudogene has been identified at 17p12-p11.
, cytokeratin 14
, keratin 14 (epidermolysis bullosa simplex, Dowling-Meara, Koebner)
, ouroboros 2
, keratin, type I cytoskeletal 14-like
, keratin, type I cytoskeletal 14
, cytokeratin VII
, epidermal keratin VII
, epidermolysis bullosa simplex, Dowling-Meara, Koebner
, keratin complex 1, acidic, gene 14
, type I keratin Ka14
, type I alpha-keratin 14
, keratin 10
, keratin 10 (epidermolytic hyperkeratosis; keratosis palmaris et plantaris)