MOSPD3 antibody

Catalog No. ABIN2463994

Product Details anti-MOSPD3 Antibody

Target: MOSPD3 (Motile Sperm Domain Containing 3 (MOSPD3))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MOSPD3 antibody is un-conjugated

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

Purification: Antibody is purified by protein A chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human MOSPD3.

Application Details

Application Notes: MOSPD3 antibody can be used for detection of MOSPD3 by ELISA at 1:1562500. MOSPD3 antibody can be used for detection of MOSPD3 by western blot at 5.0 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

Storage Comment: For short periods of storage (days) store at 4 °C. For longer periods of storage, store MOSPD3 antibody at -20 °C.

Target Details for MOSPD3

Target: MOSPD3 (Motile Sperm Domain Containing 3 (MOSPD3))

Alternative Name: MOSPD3 (MOSPD3 Products)

Synonyms: CDS3 antibody, NET30 antibody, 1190005J19Rik antibody, 5133401H10Rik antibody, Gtig2 antibody, R124 antibody, cds3 antibody, MGC89012 antibody, MOSPD3 antibody, motile sperm domain containing 3 antibody, motile sperm domain containing 3 L homeolog antibody, MOSPD3 antibody, Mospd3 antibody, mospd3 antibody, mospd3.L antibody

Background: MOSPD3 is a multi-pass membrane protein with a major sperm protein (MSP) domain. The deletion of a similar mouse gene is associated with defective cardiac development and neonatal lethality.This gene encodes a multi-pass membrane protein with a major sperm protein (MSP) domain. The deletion of a similar mouse gene is associated with defective cardiac development and neonatal lethality. Alternate transcriptional splice variants, encoding different isoforms, have been described.

Molecular Weight: 24 kDa, 26 kDa, 26 kDa, 26 kDa

Gene ID: 64598

NCBI Accession: NP_001035188

UniProt: O75425