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The protein encoded by KRT5 is a member of the keratin gene family. Additionally we are shipping Keratin 5 Proteins (13) and Keratin 5 Kits (10) and many more products for this protein.
Showing 10 out of 254 products:
Cat (Feline) Monoclonal KRT5 Primary Antibody for FACS, IHC (fro) - ABIN112348
Smedts, Ramaekers, Robben, Pruszczynski, van Muijen, Lane, Leigh, Vooijs: Changing patterns of keratin expression during progression of cervical intraepithelial neoplasia. in The American journal of pathology 1990
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Amphibian Monoclonal KRT5 Primary Antibody for EIA, FACS - ABIN112168
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 ABIN112168
Amphibian Monoclonal KRT5 Primary Antibody for IHC (fro), IF - ABIN112167
Bártek, Vojt?sek, Stasková, Bártková, Kerekés, Rejthar, Kovarík: A series of 14 new monoclonal antibodies to keratins: characterization and value in diagnostic histopathology. in The Journal of pathology 1991
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Human Monoclonal KRT5 Primary Antibody for EIA, FACS - ABIN1106933
Grin, OMalley, Mulligan: Cytokeratin 5 and estrogen receptor immunohistochemistry as a useful adjunct in identifying atypical papillary lesions on breast needle core biopsy. in The American journal of surgical pathology 2009
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Dog (Canine) Monoclonal KRT5 Primary Antibody for IHC (fro), IF - ABIN126702
Broers, Carney, Klein Rot, Schaart, Lane, Vooijs, Ramaekers: Intermediate filament proteins in classic and variant types of small cell lung carcinoma cell lines: a biochemical and immunochemical analysis using a panel of monoclonal and polyclonal antibodies. in Journal of cell science 1987
Show all 2 references for ABIN126702
Amphibian Monoclonal KRT5 Primary Antibody for FACS, IHC (fro) - ABIN112169
Waseem, Karsten, Leigh, Purkis, Waseem, Lane: Conformational changes in the rod domain of human keratin 8 following heterotypic association with keratin 18 and its implication for filament stability. in Biochemistry 2004
Show all 2 references for ABIN112169
Human Monoclonal KRT5 Primary Antibody for IHC (p) - ABIN115172
Whittock, Eady, McGrath: Genomic organization and amplification of the human epidermal type II keratin genes K1 and K5. in Biochemical and biophysical research communications 2000
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Human Monoclonal KRT5 Primary Antibody for IHC (p) - ABIN1688256
Assadi, Lamerz, Jarutat, Farfsing, Paul, Gierke, Breitinger, Templin, Essioux, Arbogast, Venturi, Pawlak, Langen, Schindler: Multiple protein analysis of formalin-fixed and paraffin-embedded tissue samples with reverse phase protein arrays. in Molecular & cellular proteomics : MCP 2013
Human Polyclonal KRT5 Primary Antibody for IF, IHC - ABIN1533561
Horrevoets, Fontijn, van Zonneveld, de Vries, ten Cate, Pannekoek et al.: Vascular endothelial genes that are responsive to tumor necrosis factor-alpha in vitro are expressed in atherosclerotic lesions, including inhibitor of apoptosis protein-1, stannin, and two novel ... in Blood 1999
data show that a cis (show CISH Antibodies)-element of the DNA segment in the CKII gene is required for epidermal cell-specific expression of CKII and that a minimal region upstream of the transcription start site is required for this expression restricted to epidermal cells
Results provide further accumulation of case series of EBS-MP and DPR (show DACT1 Antibodies) may provide more accurate diagnostic criteria for genetic disorders of the K5/K14 (show KRT14 Antibodies) pair, previously believed to be independent disorders.
The results introduce a case of special generalized DDD with a family history that clinically resembles dyschromatosis universalis hereditaria (DUH), and suggest that KRT5 may be the candidate gene.
Authors herein defined two distinct HNSCCs groups (EGFR (show EGFR Antibodies)(+) and K5(+)) with several sub-classes, identifiable by the additional assessment of p53 (show TP53 Antibodies), Bcl2 (show BCL2 Antibodies) and CD117.
identification of 29 different mutations in KRT5 and KRT14 (show KRT14 Antibodies), 11 of which were novel, in a Polish cohort of epidermolysis bullosa simplex patients
KRT5 protein mutation may predispose to a severe lethal variant of epidermolysis bullosa simplex.
study showed that 34betaE12 is the most appropriate negative marker to combine with alpha-methylacyl coenzyme A racemase (show AMACR Antibodies) as a positive marker for the diagnosis of prostate adenocarcinoma[34betaE12]
Different staining patterns can be seen with CK5/6 and p63 (show RPE65 Antibodies); however, if they are used together with TTF-1 (show NKX2-1 Antibodies) they can be used in subtyping lung neoplasms.
CK5/6 have roles in biologically aggressive tumors likely to display resistance to trastuzumab ab initio in women diagnosed with HER2 (show ERBB2 Antibodies)+ cancer
Keratinocytes adhesion and stiffness depends on KRT5 protein missense mutation.
There were differences between CK5/6, p63 (show RPE65 Antibodies),CK34betaE12 and TTF-1 (show NKX2-1 Antibodies) expression with tumor differentiation in squamous cell carcinoma or adenocarcinomas
NMHC IIA may play critical roles in the early trophoblast-derived ectoplacental cone and extraembryonic ectoderm in Keratin 5-Cre transgenic mice.
Directed expression of a chimeric type II keratin (show KRT80 Antibodies) partially rescues keratin 5 (show KRT36 Antibodies)-null mice.
NMHC IIA may play critical roles in the early trophoblast-derived ectoplacental cone and extraembryonic ectoderm in Keratin 5 (show KRT36 Antibodies)-Cre transgenic mice.
Mice lacking the prostate epithelial AR have increased apoptosis in epithelial CK8 (show KRT8 Antibodies)-positive luminal cells and increased proliferation in epithelial CK5-positive basal cells.
The involvement of Hsc70 and Hsp70 in mutant keratin degradation was demonstrated using CHIP-p.Met1_Ala142del (DeltaTPR-CHIP).
p63 (show CKAP4 Antibodies) protein is essential for the embryonic development of vibrissae and teeth; while it localizes with K5 in vibrissae, it is not fully colocalized with nuclear Ki67 (show MKI67 Antibodies) expression
keratin 5 (show KRT36 Antibodies) mutations contribute to epidermolysis bullosa simplex in a mouse model by inducing local inflammation that mediates a stress response
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.
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 basal layer of the epidermis with family member KRT14. Mutations in these genes have been associated with a complex of diseases termed epidermolysis bullosa simplex. The type II cytokeratins are clustered in a region of chromosome 12q12-q13.
keratin, type II cytoskeletal 71
, type II cytokeratin
, keratin 5 (epidermolysis bullosa simplex, Dowling-Meara/Kobner/Weber-Cockayne types)
, keratin 75
, keratin, type II cytoskeletal 5
, type II alpha keratin IIA
, 58 kda cytokeratin
, epidermolysis bullosa simplex 2 Dowling-Meara/Kobner/Weber-Cockayne types
, type-II keratin Kb5
, keratin, type II cytoskeletal 60 kDa, component III
, 58 kDa cytokeratin
, cytokeratin 5
, keratin complex 2, basic, gene 5
, tuftelin interacting protein 8
, keratin 5 (epidermolysis bullosa simplex Dowling-Meara/Kobner/Weber-Cockayne types)
, Type-II keratin Kb5