Keratin 5 rabbit pAb

Keratin 5 rabbit pAb

AO-06-ES8918-50

Keratin 5 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES8918
Product nameKeratin 5 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC
Other nameKeratin, type II cytoskeletal 5 (58 kDa cytokeratin) (Cytokeratin-5) (CK-5) (Keratin-5) (K5) (Type-II keratin Kb5)
Size50μL
Unit price ($)148
Human gene ID3852
Human Swiss-ProtP13647
SourceRabbit
IsotypeIgG
TargetCytokeratin 5
Fields
Gene nameKRT5
Protein nameKeratin, type II cytoskeletal 5 (58 kDa cytokeratin) (Cytokeratin-5) (CK-5) (Keratin-5) (K5) (Type-II keratin Kb5)
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID110308
Mouse gene link
Mouse Swiss-ProtQ922U2
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID369017
Rat gene link
Rat Swiss-ProtQ6P6Q2
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from human Keratin 5 Polyclonal
SpecificityThis antibody detects endogenous levels of Keratin 5.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)62kD
Backgroundkeratin 5(KRT5) Homo sapiens 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. [provided by RefSeq, Jul 2008],
Functiondisease:Defects in KRT5 are a cause of epidermolysis bullosa simplex Dowling-Meara type (DM-EBS) [MIM:131760]. DM-EBS is a severe form of intraepidermal epidermolysis bullosa characterized by generalized herpetiform blistering, milia formation, dystrophic nails, and mucous membrane involvement.,disease:Defects in KRT5 are a cause of epidermolysis bullosa simplex Koebner type (K-EBS) [MIM:131900]. K-EBS is a form of intraepidermal epidermolysis bullosa characterized by generalized skin blistering. The phenotype is not fundamentally distinct from the Dowling-Meara type, althought it is less severe.,disease:Defects in KRT5 are a cause of epidermolysis bullosa simplex Weber-Cockayne type (WC-EBS) [MIM:131800]. WC-EBS is a form of intraepidermal epidermolysis bullosa characterized by blistering limited to palmar and plantar areas of the skin.,disease:Defects in KRT5 are the cause of Dowling-D
Subcellular locationnucleus,cytoplasm,mitochondrion,cytosol,intermediate filament,plasma membrane,membrane,keratin filament,extracellular exosome,
ExpressionExpressed in corneal epithelium (at protein level).

Additional Images

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Western blot analysis of SW480 lysate, antibody was diluted at 1000. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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Immunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
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: AO-06-ES8918-50
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Hurry! only 10 items left in stock.

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