Cytokeratin 5 Antikörper (truncated)
Kurzübersicht für Cytokeratin 5 Antikörper (truncated) (ABIN2464042)
Target
Alle Cytokeratin 5 (KRT5) Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
Klon
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Bindungsspezifität
- truncated
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Immunogen
- Ni-NTA purified truncated recombinant CK5-Trx-His expressed in E. Coli strain BL21 (DE3).
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Isotyp
- IgG1
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Applikationshinweise
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Western Blot:1:500 - 1:2,000
IHC(P):1:500 - 1:2,000
ELISA:Propose dilution 1:10,000.
Determining optimal working dilutions by titration test. -
Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Buffer
- Ascitic fluid containing 0.03 % sodium azide.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handhabung
- As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Cytokeratin 5 monoclonal antibody can be stored at -20 °C, stable for one year.
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- Cytokeratin 5 (KRT5) (Keratin 5 (KRT5))
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Andere Bezeichnung
- Cytokeratin5
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Hintergrund
- CK5 (keratin 5) is a member of the keratin gene family. Biochemically, most members of the CK family fall into one of two classes, type I (acidic polypeptides) and type II (basic polypeptides). 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. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. At least one member of the acidic family and one member of the basic family is expressed in all epithelial cells. Cytokeratin 5 is expressed in normal basal cells. Mutations of the Cytokeratin5 gene (KRT5) have been shown to result in the autosomal dominant disorderepidermolysis bullosa (EB). Defects in KRT5 are a cause of epidermolysis bullosa simplex.
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Gen-ID
- 3852
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UniProt
- P13647
Target
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