Product name: Cytokeratin 10 (1D8) Monoclonal Antibody
Applications: WB, IHC-P, IF(ICC)
Reactivity: Human, Mouse, Rat
Conjugation: Unconjugated
Host: Rabbit
Source: Recombinant human Cytokeratin 10 protein, around 150-250aa.
Clonality: Monoclonal
Clone: #1D8
Isotype: IgG
Concentration: 1ug/ul
Purification: Purified by Protein A.
Storage buffer: Aqueous buffered solution containing 1xTBS (pH7.4), 1%BSA, 40%Glycerol and 0.05% Sodium Azide.
Storage condition: Store at -20°C for 12 months
TARGET
Gene ID: 3858
Swiss Prot: P13645
Synonyms: BIE; EHK; K10; KPP; BCIE; CK10; Keratin, type I cytoskeletal 10; Cytokeratin-10; CK-10; Keratin-10; KRT10
Background: Cytokeratin 10 is a heterotetramer of two type I and two type II keratins. Cytokeratin 10 is generally associated with keratin 1. It is seen in all suprabasal cell layers including stratum corneum. A number of alleles are known that mainly differ in the Gly-rich region (positions 490-560). Defects in cytokeratin 10 are a cause of epidermolytic hyperkeratosis (EHK), also known as bullous congenital ichthyosiform erythroderma (BCIE) or bullous erythroderma ichthyosiformis congenita of Brocq. EHK is an hereditary skin disorder characterized by blistering and a marked thickening of the stratum corneum. At birth, affected individuals usually present with redness, blisters and superficial erosions due to cytolysis. Within a few weeks, the erythroderma and blister formation diminish and hyperkeratoses develop. Transmission is autosomal dominant, but most cases are sporadic. Defects in cytokeratin 10 are also a cause of annular epidermolytic ichthyosis (AEI), also known as cyclic ichthyosis with epidermolytic hyperkeratosis. AEI resembles clinical and histologic features of both epidermolytic hyperkeratosis and ichthyosis bullosa of Siemens.
*Image title: HeLa lysates; probed with Cytokeratin 10 (1D8) Monoclonal Antibody (bsm-52052R) at 1:1000 overnight at 4˚C. Followed by a conjugated secondary antibody.
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