RBM10 antibody

Catalog No. ABIN7230972

This Rabbit Polyclonal antibody specifically detects RBM10 in ELISA and WB. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for RBM10 antibody (ABIN7230972)

Target: RBM10 (RNA Binding Motif Protein 10 (RBM10))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RBM10 antibody is un-conjugated

Application: ELISA, Western Blotting (WB)

Product Details anti-RBM10 Antibody

Purpose: Rabbit Anti-RBM10 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of RBM10 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human RBM10 protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for RBM10

Target: RBM10 (RNA Binding Motif Protein 10 (RBM10))

Alternative Name: RBM10

Background: RNA-binding protein 10, G patch domain-containing protein 9, RNA-binding motif protein 10, RNA-binding protein S1-1, S1-1RBM10 gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.

Molecular Weight: 102kD

Gene ID: 8241

UniProt: P98175