Cytokeratin 14 (CK14) (ABT214R) rabbit mAb

  • Catalog No.：YM7096
  • Applications：IHC;WB; ELISA
  • Reactivity：Human; (predicted: Mouse; Rat)
    • Target：
    • Cytokeratin 14
    • Fields：
    • >>Estrogen signaling pathway;>>Staphylococcus aureus infection
    • Gene Name：
    • KRT14
    • Protein Name：
    • Keratin, type I cytoskeletal 14 (Cytokeratin-14) (CK-14) (Keratin-14) (K14)
    • Human Gene Id：
    • 3861
    • Human Swiss Prot No：
    • P02533
    • Immunogen：
    • Synthesized peptide derived from human Cytokeratin 14 AA range:400-472
    • Specificity：
    • This antibody detects endogenous levels of Cytokeratin 14
    • Formulation：
    • PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
    • Source：
    • Monoclonal, Rabbit IgG1, Kappa
    • Dilution：
    • IHC 1:100-500, WB 1:500-1000, ELISA 1:5000-20000
    • Purification：
    • Recombinant Expression and Affinity purified
    • Storage Stability：
    • -15°C to -25°C/1 year(Do not lower than -25°C)
    • Other Name：
    • CK 14;CK-14;ck14;Cytokeratin 14;CytokeRatin-14;CytokeRatin14;Dowling Meara;EBS3;EBS4;Epidermolysis bullosa simplex;K14;K1C14_HUMAN;KeRatin 14 (epidermolysis bullosa simplex, Dowling-Meara, Koebner);KeRatin 14;KeRatin;KeRatin type I cytoskeletal 14;KeRatin, type I cytoskeletal 14;KeRatin-14;KeRatin14;Koebner;Krt 14;Krt14;NFJ;OTTHUMP00000164624;type I cytoskeletal 14
    • Molecular Weight(Da)：
    • 52kD
    • Background：
    • This gene encodes a member of the keratin family, the most diverse group of intermediate filaments. This gene product, a type I keratin, is usually found as a heterotetramer with two keratin 5 molecules, a type II keratin. Together they form the cytoskeleton of epithelial cells. Mutations in the genes for these keratins are associated with epidermolysis bullosa simplex. At least one pseudogene has been identified at 17p12-p11. [provided by RefSeq, Jul 2008],
    • Function：
    • disease:Defects in KRT14 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 KRT14 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 KRT14 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 KRT14 are the cause of derma
    • Subcellular Location：
    • Cytoplasmic, Membranous
    • Expression：
    • Expressed in the corneal epithelium (at protein level) (PubMed:26758872). Detected in the basal layer, lowered within the more apically located layers specifically in the stratum spinosum, stratum granulosum but is not detected in stratum corneum. Strongly expressed in the outer root sheath of anagen follicles but not in the germinative matrix, inner root sheath or hair (PubMed:9457912). Found in keratinocytes surrounding the club hair during telogen (PubMed:9457912).

    Attributes

    • Code：
    • YM7096
    • Size
    • 40μL / 100μL / 200μL
    • Price$：
    • 190 / 340 / 600
    • Delivery：
    • 2024-07-04
    Order

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