ROR2 Antibody (SR1037) - BSA Free

Western Blot: ROR2 Antibody (SR1037) [NBP3-22166] - Western blot analysis using NBP3-22166 in Saos-2 cell lysate.

• Reactivity: Hu
• Applications: WB, Flow, ICC/IF
• Clone: SR1037
• Clonality: Monoclonal
• Host: Rabbit
• Conjugate: Unconjugated
• Format: BSA Free

ROR2 Antibody (SR1037) - BSA Free Summary

• Description: Novus Biologicals Rabbit ROR2 Antibody (SR1037) - BSA Free (NBP3-22166) is a recombinant monoclonal antibody validated for use in WB, Flow and ICC/IF. All Novus Biologicals antibodies are covered by our 100% guarantee.
• Additional Information: Recombinant Monoclonal Antibody
• Immunogen: A synthesized peptide derived from human ROR2 (Uniprot #: Q01974)
• Specificity: Detects endogenous levels of total ROR2
• Source: HEK293
• Isotype: IgG
• Clonality: Monoclonal
• Host: Rabbit
• Gene: ROR2
• Purity: Affinity purified

Applications/Dilutions

• Dilutions:
  • Flow Cytometry 1:50
  • Immunocytochemistry/ Immunofluorescence 1:50-1:200
  • Western Blot 1:500-1:2000
• Theoretical MW: 105 kDa.
  Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

• Storage: Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
• Buffer: PBS, pH 7.4, 150mM NaCl, 50% glycerol.
• Preservative: 0.02% Sodium Azide
• Purity: Affinity purified

Alternate Names for ROR2 Antibody (SR1037) - BSA Free

• 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