ASPM anticorps (C-Term)

N° du produit ABIN7448380

Cet anticorps Lapin Polyclonal détecte spécifiquement ASPM dans IF/ICC. Il présente une réactivité envers Humain.

Aperçu rapide pour ASPM anticorps (C-Term) (ABIN7448380)

Antigène: ASPM (Asp (Abnormal Spindle) Homolog, Microcephaly Associated (ASPM))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ASPM est non-conjugé

Application: Immunofluorescence (fixed cells) (IF/ICC)

Détail du produit anti-ASPM anticorps

Épitope: C-Term

Fonction: Rabbit anti-ASPM IHC Antibody, Affinity Purified

Purification: Affinity Purified

Immunogène: Between AA 3425 and C-term

Isotype: IgG

Information d'application

Indications d'application: 1:100 - 1:500

Restrictions: For Research Use only

Stockage

Concentration: 250 μg/mL

Buffer: Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

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: 4 °C

Date de péremption: 12 months

Détails sur ASPM

Antigène: ASPM (Asp (Abnormal Spindle) Homolog, Microcephaly Associated (ASPM))

Autre désignation: ASPM

Sujet: Background: ASPM (abnormal spindle-like microcephaly associated) is also known as MCPH5 (autosomal recessive primary microcephaly 5). Defects in ASPM are the cause of microcephaly primary type 5 or microcephaly vera, an autosomal recessive disease characterized by reduced head circumference, small cerebral cortex, and reduced brain weight. At the cellular level, MCPH5 is important to mitotic spindle function and may play a preferential role in prenatal neurogenesis.

ID gène: 259266

NCBI Accession: NP_060606

UniProt: Q8IZT6