MOSPD3 anticorps

N° du produit ABIN2463994

Détail du produit anti-MOSPD3 anticorps

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MOSPD3 est non-conjugé

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

Purification: Antibody is purified by protein A chromatography method.

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

Information d'application

Indications d'application: 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

Stockage

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.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

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

Détails sur MOSPD3

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

Autre désignation: MOSPD3 (MOSPD3 Produits)

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

Sujet: 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.

Poids moléculaire: 24 kDa, 26 kDa, 26 kDa, 26 kDa

ID gène: 64598

NCBI Accession: NP_001035188

UniProt: O75425