MOSPD2 antibody (AA 111-496) (Biotin)

Catalog No. ABIN8011686

The Rabbit Polyclonal anti-MOSPD2 antibody is suitable to detect MOSPD2 in samples from Human, Mouse and Rat. It has been validated for WB, IHC and ELISA.

Quick Overview for MOSPD2 antibody (AA 111-496) (Biotin) (ABIN8011686)

Target: MOSPD2 (Motile Sperm Domain Containing 2 (MOSPD2))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MOSPD2 antibody is conjugated to Biotin

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

Product Details anti-MOSPD2 Antibody (Biotin)

Binding Specificity: AA 111-496

Purpose: Anti-MOSPD2 Antibody Biotin Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human MOSPD2 recombinant protein (Position: R111-Q496).

Isotype: IgG

Application Details

Application Notes: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for MOSPD2

Target: MOSPD2 (Motile Sperm Domain Containing 2 (MOSPD2))

Alternative Name: MOSPD2

Background:

Background: MOSPD2 (motile sperm domain-containing protein 2) is a 518 amino acid single-pass membrane protein that contains one CRAL-TRIO domain and a single MSP domain. Existing as two alternatively spliced isoforms, MOSPD2 is encoded by a gene that maps to human chromosome Xp22.2. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

Gene Full Name: motile sperm domain containing 2

Gene ID: 158747

UniProt: Q8NHP6