CCT5 anticorps (AA 442-541)

N° du produit ABIN7825310

Cet anticorps anti-CCT5 est un anticorps Polyclonal produit chez le Lapin, détectant CCT5 dans WB. Convient pour Poisson zèbre (Danio rerio).

Aperçu rapide pour CCT5 anticorps (AA 442-541) (ABIN7825310)

Antigène: CCT5 (Chaperonin Containing TCP1, Subunit 5 (Epsilon) (CCT5))

Reactivité: Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCT5 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-CCT5 anticorps

Épitope: AA 442-541

Fonction: Anti-Zebrafish CCT5 Antibody

Attributs du produit: Anti-Zebrafish CCT5 Antibody catalog # AZQ6NVI6. Tested in WB applications. This antibody reacts with Zebrafish. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived zebrafish CCT5 recombinant protein (Position: S442-D541).

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Zebrafish

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Détails sur CCT5

Antigène: CCT5 (Chaperonin Containing TCP1, Subunit 5 (Epsilon) (CCT5))

Autre désignation: CCT5

Sujet: CCT5 is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Mutations in this gene cause hereditary sensory and autonomic neuropathy with spastic paraplegia (HSNSP). Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 5 and 13.

ID gène: 322258