CEP152 anticorps (AA 901-1000)

N° du produit ABIN872433

Cet anticorps anti-CEP152 est un anticorps Lapin Polyclonal détectant CEP152 dans ELISA, WB, IF (cc), IF (p), IHC (fro) et IHC (p). Adapté pour Humain.

Aperçu rapide pour CEP152 anticorps (AA 901-1000) (ABIN872433)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CEP152 est non-conjugé

Application: ELISA, Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-CEP152 anticorps

Épitope: AA 901-1000

Homologie: Human,Mouse,Rat,Dog,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CEP152

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur CEP152

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

Autre désignation: CEP152

Sujet:

Synonyms: CE152_HUMAN, Centrosomal protein 152 kDa, Centrosomal protein of 152 kDa, Cep152, FLJ21594, KIAA0912, MCPH4.

Background: Defects in CEP152 are the cause of microcephaly primary type 4 (MCPH4). A disease defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Affected individuals are mentally retarded. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits due to degenerative brain disorder.

ID gène: 22995

Pathways: M Phase