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Upingbio
SKU:YP-Ab-15513-53UL
Cytokeratin 5 (CK5) rabbit mAb(ABT168R)
Cytokeratin 5 (CK5) rabbit mAb(ABT168R)
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- Reaction species: Human
- Gene Name: KRT5
- Protein name: Cytokeratin 5 (CK5)
- Immunogen: Synthesized peptide derived from human Cytokeratin 5 (CK5)
- Specificity: This antibody detects endogenous levels of Cytokeratin 5 (CK5) at Human
- Composition: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
- Source: Polyclonal, Rabbit,IgG
- Dilution ratio: IHC-p 1:50-1:200. IF 1:50-200
- Purification process: The antibody was affinity-purified from Cell supernatant by affinity-chromatography using specific immunogen.
- Storage: -20°C/1 year
- Other Names: Keratin, type II cytoskeletal 5 (58 kDa cytokeratin;Cytokeratin-5;CK-5;Keratin-5;K5;Type-II keratin Kb5)
- Function: disease: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
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