ASPM antibody (C-Term)

Catalog No. ABIN7448380

Product Details anti-ASPM Antibody

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

Binding Specificity: C-Term

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ASPM antibody is un-conjugated

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

Purpose: Rabbit anti-ASPM IHC Antibody, Affinity Purified

Purification: Affinity Purified

Immunogen: Between AA 3425 and C-term

Isotype: IgG

Application Details

Application Notes: 1:100 - 1:500

Restrictions: For Research Use only

Handling

Concentration: 250 μg/mL

Buffer: Tris-buffered Saline containing 0.1 % BSA and 0.09 % 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: 4 °C

Expiry Date: 12 months

Target Details for ASPM

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

Alternative Name: ASPM (ASPM Products)

Synonyms: Calmbp1 antibody, ASPM antibody, ASP antibody, MCPH5 antibody, D330028K02Rik antibody, Sha1 antibody, abnormal spindle microtubule assembly antibody, asp (abnormal spindle)-like, microcephaly associated (Drosophila) antibody, Aspm antibody, ASPM antibody, aspm antibody

Background: 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.

Gene ID: 259266

NCBI Accession: NP_060606

UniProt: Q8IZT6