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Cytokeratin 10 mouse mAb(ABT056)

Refer to | for labeled antibodies

Specification

BYab-17637

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Product introduction Experimental scheme Citation Related products

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Host
Reactiveness
Use
Molecular weight (DA)
Immunogen
Synthesized peptide derived from human CK10
Specificity
The antibody can specifically recognize human CK10 protein, and shows no cross reaction with CK4, 5, 6, 7, 8, 14, 15, 18, 19.
Source
Mouse, Monoclonal/IgG1, Kappa
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.90% sodium azide.
Dilution rate
IHC-p 1:100-500, IF 1:100-500
Purification process (Immunogen)
The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
Concentration
Background
This gene encodes a member of the type I (acidic) cytokeratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. Mutations in this gene are associated with epidermolytic hyperkeratosis. This gene is located within a cluster of keratin family members on chromosome 17q21. [provided by RefSeq, Jul 2008],
Function
disease:Defects in KRT10 are a cause of bullous congenital ichthyosiform erythroderma (BCIE) [MIM:113800]; also known as epidermolytic hyperkeratosis (EHK) or bullous erythroderma ichthyosiformis congenita of Brocq. BCIE is an autosomal dominant skin disorder characterized by widespread blistering and an ichthyotic erythroderma at birth that persist into adulthood. Histologically there is a diffuse epidermolytic degeneration in the lower spinous layer of the epidermis. Within a few weeks from birth, erythroderma and blister formation diminish and hyperkeratoses develop.,disease:Defects in KRT10 are a cause of epidermal nevus epidermolytic hyperkeratotic type [MIM:600648]. Epidermal nevi affect about 1 in 1,000 people. They appear at or shortly after birth as localized lines of epidermal thickening. The extent of skin involvement varies widely.,disease:Defects in KRT10 are a cause of icht
Gene Name
KRT10 KPP
Protein name
Cytokeratin-10
Abbreviation
Cytokeratin 10
Other name
Keratin, type I cytoskeletal 10 (Cytokeratin-10;CK-10;Keratin-10;K10)
Fields
>>Estrogen signaling pathway;>>Staphylococcus aureus infection
Human gene ID
3858
Human protein sequence Database
P13645
Mouse gene ID
Mouse protein sequence database
Rat gene ID
Rat protein sequence database
Cellular localization
Secreted, extracellular space . Cell surface . Localized on the surface of desquamated nasal epithelial cells (PubMed:12427098). Localized on the surface of lung cell lines (PubMed:19627498). .
Tissue expression
Seen in all suprabasal cell layers including stratum corneum. Expressed on the surface of lung cell lines (PubMed:19627498).
Storage
-20°C/1 year

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Cytokeratin 10 mouse mAb(ABT056)

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