Cullin 7 anticorps (AA 1570-1650)

N° du produit ABIN7228102

L’anticorps Lapin Polyclonal anti-Cullin 7 a été validé pour WB et ELISA. Il convient pour détecter Cullin 7 dans des échantillons de Humain et Souris.

Aperçu rapide pour Cullin 7 anticorps (AA 1570-1650) (ABIN7228102)

Antigène: Cullin 7 (CUL7)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Cullin 7 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Cullin 7 anticorps

Épitope: AA 1570-1650

Fonction: CUL7 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of CUL7 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogène: Synthesized peptide derived from part region of human CUL7 protein at AA range: 1570-1650

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur Cullin 7

Antigène: Cullin 7 (CUL7)

Autre désignation: CUL7

Sujet: Rabbit Anti-CUL7 Polyclonal Antibody,Cullin-7, CUL-7,The protein encoded by CUL7 (Cullin 7) is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in CUL7 are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for CUL7. CUL7 is a Protein Coding gene. Diseases associated with CUL7 include 3-M Syndrome 1 and 3-M Syndrome, Cul7-Related. Among its related pathways are Class I MHC mediated antigen processing and presentation and Unfolded Protein Response (UPR).,CUL7

Poids moléculaire: observerd band 186kDa

ID gène: 9820

UniProt: Q14999

Pathways: ER-Nucleus Signaling