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The protein encoded by KRT5 is a member of the keratin gene family. 再加上，我们可以发Keratin 5 蛋白 (16) 和 Keratin 5 试剂盒 (12)和数多这个蛋白质的别的产品。
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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
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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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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
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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 FACS, IHC (p) - ABIN1688226
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 (显示 CISH 抗体)-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
CK5 and p40 (显示 IL9 抗体) are good diagnostic markers for squamous cell carcinoma and superior to p63 (显示 RPE65 抗体)
The expression of CK5/6 and of P63 (显示 RPE65 抗体) suggests a squamous differentiation including in the basaloid thyroid lymphoepithelial complexes
Immunocytochemistry using this antibody cocktail comprises five antibodies recognising p63 (显示 RPE65 抗体), and cytokeratins ( 7, 18, 5 and 14) showed good sensitivity and specificity for diagnosing breast cancers. Thus, this method is useful for mammary cytology using FNA
the consistency test results indicated the inter-observer agreement was more robust in MS images for HER2 (显示 ERBB2 抗体) , CK5/6 and ER than that in RGB images for HER2 (显示 ERBB2 抗体) , CK5/6 and ER .
the luminal cells of adenoid cystic carcinoma show a unique aberrant staining pattern for cytokeratin 5/6 that may aid in the differential diagnosis
Results provide further accumulation of case series of EBS-MP and DPR (显示 DACT1 抗体) may provide more accurate diagnostic criteria for genetic disorders of the K5/K14 (显示 KRT14 抗体) 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 (显示 EGFR 抗体)(+) and K5(+)) with several sub-classes, identifiable by the additional assessment of p53 (显示 TP53 抗体), Bcl2 (显示 BCL2 抗体) and CD117.
identification of 29 different mutations in KRT5 and KRT14 (显示 KRT14 抗体), 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.
NMHC IIA may play critical roles in the early trophoblast-derived ectoplacental cone and extraembryonic ectoderm in Keratin 5-Cre transgenic mice.
Loss of activating transcription factor 3 (ATF3 (显示 ATF3 抗体)) in knockout mice promotes the emergence of keratins CK5+CK8 (显示 KRT8 抗体)+ epithelial cells.
Directed expression of a chimeric type II keratin (显示 KRT80 抗体) partially rescues keratin 5 (显示 KRT36 抗体)-null mice.
NMHC IIA may play critical roles in the early trophoblast-derived ectoplacental cone and extraembryonic ectoderm in Keratin 5 (显示 KRT36 抗体)-Cre transgenic mice.
Mice lacking the prostate epithelial AR have increased apoptosis in epithelial CK8 (显示 KRT8 抗体)-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 (显示 CKAP4 抗体) 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 (显示 MKI67 抗体) expression
keratin 5 (显示 KRT36 抗体) 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 (显示 CKAP4 抗体) 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