ROR2 antibody (Biotin)

Catalog No. ABIN7851495

The Biotin-conjugated Rabbit Monoclonal anti-ROR2 antibody (Clone DM174) (ABIN7851495) specifically detects ROR2 in WB, ELISA and FACS. The antibody is reactive with Human samples.

Quick Overview for ROR2 antibody (Biotin) (ABIN7851495)

Target: ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))

Reactivity: Human

Host: Rabbit

Clonality: Monoclonal

Conjugate: This ROR2 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Clone: DM174

Product Details anti-ROR2 Antibody (Biotin)

Purpose: Biotinylated Anti-ROR2 antibody(DM174), Rabbit mAb

Purification: Purified from cell culture supernatant by affinity chromatography

Isotype: IgG

Application Details

Application Notes: ELISA 1:5000-10000, Flow Cyt 1:100, WB 1:1000

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Please see Certificate of Analysis for specific instructions of reconstitution.

Buffer: Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

Storage: -20 °C,-80 °C

Storage Comment: Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

Expiry Date: 12 months

Target Details for ROR2

Target: ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))

Alternative Name: ROR2

Background: The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia:aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.

UniProt: Q01974

Pathways: RTK Signaling, WNT Signaling