CEP41 antibody (AA 150-200)

Catalog No. ABIN1451148

The Rabbit Polyclonal anti-CEP41 antibody (ABIN1451148) specifically detects CEP41 in IHC, ELISA and IF. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for CEP41 antibody (AA 150-200) (ABIN1451148)

Target: CEP41 (Centrosomal Protein 41kDa (CEP41))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CEP41 antibody is un-conjugated

Application: Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Product Details anti-CEP41 Antibody

Binding Specificity: AA 150-200

Purpose: CEP41 Antibody

Specificity: CEP41 Polyclonal Antibody detects endogenous levels of CEP41 protein.

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

Purity: > 95 %

Immunogen: The antiserum was produced against synthesized peptide derived from human CEP41. AA range:150-200

Isotype: IgG

Application Details

Application Notes: 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: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for CEP41

Target: CEP41 (Centrosomal Protein 41kDa (CEP41))

Alternative Name: CEP41

Background:

Synonyms: CEP41, TSGA14, Centrosomal protein of 41 kDa, Cep41, Testis-specific gene A14 protein

Background: This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15, an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012],

Gene Name: CEP41

Protein Name: Centrosomal protein of 41 kDa

Molecular Weight: 41 kDa

Gene ID: 95681

OMIM: 610523

UniProt: Q9BYV8

Pathways: M Phase