ROR2 Antibody (0B7X8)

Novus Biologicals | Catalog # NBP3-16564

Recombinant Monoclonal Antibody
Novus Biologicals
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Key Product Details

Species Reactivity

Mouse

Applications

Western Blot

Label

Unconjugated

Antibody Source

Recombinant Monoclonal Rabbit IgG Clone # 0B7X8 expressed in HEK293
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Product Specifications

Immunogen

A synthetic peptide corresponding to a sequence within amino acids 1-100 of human ROR2 (Q01974). MARGSALPRRPLLCIPAVWAAAALLLSVSRTSGEVEVLDPNDPLGPLDGQDGPIPTLKGYFLNFLEPVNNITIVQGQTAILHCKVAGNPPPNVRWLKNDA

Clonality

Monoclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for ROR2 Antibody (0B7X8)

Western Blot: ROR2 Antibody (0B7X8) [NBP3-16564]

Western Blot: ROR2 Antibody (0B7X8) [NBP3-16564]

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.

Applications for ROR2 Antibody (0B7X8)

Application
Recommended Usage

Western Blot

1:500 - 1:2000

Formulation, Preparation, and Storage

Purification

Affinity purified

Formulation

PBS (pH 7.3), 50% glycerol, 0.05% BSA

Preservative

0.02% Sodium Azide

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at -20C. Avoid freeze-thaw cycles.

Background: ROR2

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.

Long Name

Receptor Tyrosine Kinase-like Orphan Receptor 2

Alternate Names

BDB1, NTRKR2

Gene Symbol

ROR2

Additional ROR2 Products

Product Documents for ROR2 Antibody (0B7X8)

Certificate of Analysis

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Product Specific Notices for ROR2 Antibody (0B7X8)

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.

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