CCDC8 Antikörper (AA 165-270)

Produktnummer ABIN872904

Produktdetails anti-CCDC8 Antikörper

Target: CCDC8 (Coiled-Coil Domain Containing 8 (CCDC8))

Bindungsspezifität: AA 165-270

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCDC8 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Kreuzreaktivität: Human, Maus

Homologie: Rat,Dog,Pig,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC8

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Haltbarkeit: 12 months

Details zu CCDC8

Target: CCDC8 (Coiled-Coil Domain Containing 8 (CCDC8))

Andere Bezeichnung: CCDC8 (CCDC8 Produkte)

Synonyme: 3M3 antikoerper, PPP1R20 antikoerper, p90 antikoerper, ENSMUSG00000041117 antikoerper, coiled-coil domain containing 8 antikoerper, CCDC8 antikoerper, Ccdc8 antikoerper

Hintergrund:

Synonyms: CCDC8, CCDC8_HUMAN, Coiled-coil domain-containing protein 8, DKFZp564K0322, ENSMUSG00000041117, MGC72567.

Background: This gene encodes a coiled-coil domain-containing protein. The encoded protein functions as a cofactor required for p53-mediated apoptosis following DNA damage, and may also play a role in growth through interactions with the cytoskeletal adaptor protein obscurin-like 1. Mutations in this gene are a cause of 3M syndrome-3 (3M3). [provided by RefSeq, Dec 2011].

Gen-ID: 83987