Cullin 4A anticorps (AA 590-670)

N° du produit ABIN7228098

L’anticorps anti-Cullin 4A Polyclonal Lapin est utilisé pour la détection de Cullin 4A dans des échantillons de Humain et Souris. Il a été validé pour WB et ELISA.

Aperçu rapide pour Cullin 4A anticorps (AA 590-670) (ABIN7228098)

Antigène: Cullin 4A (CUL4A)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Cullin 4A est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Cullin 4A anticorps

Épitope: AA 590-670

Fonction: Rabbit Anti-CUL4A Polyclonal Antibody

Specificité: The antibody detects endogenous levels of CUL4A protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from part region of human CUL4A protein at AA range: 590-670

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 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

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: 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.

Date de péremption: 12 months

Détails sur Cullin 4A

Antigène: Cullin 4A (CUL4A)

Autre désignation: CUL4A

Sujet: Cullin-4A, CUL-4ACUL4A (Cullin 4A) is the ubiquitin ligase component of a multimeric complex involved in the degradation of DNA damage-response proteins. CUL4A is a Protein Coding gene. Diseases associated with CUL4A include Xeroderma Pigmentosum Group E and Xeroderma Pigmentosum, Variant Type. Among its related pathways are Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template and Transcription-Coupled Nucleotide Excision Repair (TC-NER).

Poids moléculaire: 83kD

ID gène: 8451

UniProt: Q13619