CEP152 antibody (AA 810-890)

Catalog No. ABIN7220602

The Rabbit Polyclonal anti-CEP152 antibody is suitable to detect CEP152 in samples from Human and Mouse. It has been validated for ELISA, WB, IHC and IF.

Quick Overview for CEP152 antibody (AA 810-890) (ABIN7220602)

Target: CEP152 (Centrosomal Protein 152kDa (CEP152))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CEP152 antibody is un-conjugated

Application: ELISA, Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Product Details anti-CEP152 Antibody

Binding Specificity: AA 810-890

Purpose: Rabbit Anti-CEP152 Polyclonal Antibody

Specificity: CEP152 Polyclonal Antibody detects endogenous levels of CEP152 protein.

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

Immunogen: Synthesized peptide derived from the Internal region of human CEP152 at AA range: 810-890

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,IHC 1:100-1:300,ELISA 1:40000,IF 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: 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.

Expiry Date: 12 months

Target Details for CEP152

Target: CEP152 (Centrosomal Protein 152kDa (CEP152))

Alternative Name: CEP152

Background: CEP152, KIAA0912, Centrosomal protein of 152 kDa, Cep152CEP152 encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in multiple transcript variants.

Molecular Weight: 140kD

Gene ID: 22995

UniProt: O94986

Pathways: M Phase