CCDC8 anticorps (AA 165-270) (AbBy Fluor® 647)

N° du produit ABIN888137

L’anticorps Lapin Polyclonal anti-CCDC8 a été validé pour WB, IF (cc) et IF (p). Il convient pour détecter CCDC8 dans des échantillons de Humain et Souris.

Aperçu rapide pour CCDC8 anticorps (AA 165-270) (AbBy Fluor® 647) (ABIN888137)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC8 est conjugé à/à la AbBy Fluor® 647

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-CCDC8 anticorps (AbBy Fluor® 647)

Épitope: AA 165-270

Réactivité croisée: Humain, Souris

Homologie: Rat,Dog,Pig,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CCDC8

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur CCDC8

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

Autre désignation: CCDC8

Sujet:

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].

ID gène: 83987