ROR2 Antibody (0B7X8)

Western Blot: ROR2 Antibody (0B7X8) [NBP3-16564] - Western blot analysis of extracts of various cell lines, using ROR2 Rabbit mAb (NBP3-16564) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit. Exposure time: 90s.

• Reactivity: Mu
• Applications: WB
• Clone: 0B7X8
• Clonality: Monoclonal
• Host: Rabbit
• Conjugate: Unconjugated

ROR2 Antibody (0B7X8) Summary

• Description: Novus Biologicals Rabbit ROR2 Antibody (0B7X8) (NBP3-16564) is a recombinant monoclonal antibody validated for use in WB. All Novus Biologicals antibodies are covered by our 100% guarantee.
• Additional Information: Recombinant Monoclonal Antibody
• Immunogen: A synthetic peptide corresponding to a sequence within amino acids 1-100 of human ROR2 (Q01974). MARGSALPRRPLLCIPAVWAAAALLLSVSRTSGEVEVLDPNDPLGPLDGQDGPIPTLKGYFLNFLEPVNNITIVQGQTAILHCKVAGNPPPNVRWLKNDA
• Source: HEK293
• Isotype: IgG
• Clonality: Monoclonal
• Host: Rabbit
• Gene: ROR2
• Purity: Affinity purified

Applications/Dilutions

• Dilutions:
  • Western Blot 1:500 - 1:2000

Packaging, Storage & Formulations

• Storage: Store at -20C. Avoid freeze-thaw cycles.
• Buffer: PBS (pH 7.3), 50% glycerol, 0.05% BSA
• Preservative: 0.02% Sodium Azide
• Purity: Affinity purified

Alternate Names for ROR2 Antibody (0B7X8)

• BDB
• BDB1
• EC 2.7.10.1
• MGC163394
• neurotrophic tyrosine kinase receptor-related 2
• Neurotrophic tyrosine kinase, receptor-related 2
• NTRKR2
• NTRKR2tyrosine-protein kinase transmembrane receptor ROR2
• receptor tyrosine kinase-like orphan receptor 2
• ROR2

Background

ROR2 is 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.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Bioinformatics

• Gene Symbol: ROR2