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ROR2 antibody (Receptor Tyrosine Kinase-Like Orphan Receptor 2)

Details for Product anti-ROR2 Antibody No. ABIN392046, Supplier: Login to see New
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Synonyms ROR2, bdb, bdb1, Xror2, ntrkr2, MGC97773, LOC100219935, BDB, BDB1, NTRKR2, Ntrkr2, mRor2
(95), (10), (6), (2), (2), (2), (1)
(81), (14), (1)
Clonality (Clone)
Polyclonal ()
This ROR2 antibody is un-conjugated
(6), (6), (5), (4), (4), (4)
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
(75), (47), (45), (25), (9), (5), (3), (2), (2), (1)
Pubmed 6 references available
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Quantity 400 μL
Shipping to United States ( )
Availability Will be delivered in 2 to 4 Business Days
Immunogen This ROR2 antibody is generated from rabbits immunized with a recombinant protein of human ROR2.
Clone RB16733
Isotype Ig
Specificity This ROR2 antibody is generated from rabbits immunized with a recombinant protein of human ROR2.
Purification This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
Alternative Name ROR2 (ROR2 Antibody Abstract)
Background ROR2 is a tyrosine-protein kinase receptor which may be involved in the early formation of the chondrocytes. It seems to be required for cartilage and growth plate development. This Type I membrane protein is expressed at high levels during early embryonic development. The expression levels drop strongly around day 16 and there are only very low levels in adult tissues. Defects in ROR2 are a cause of brachydactyly type B1 (BDB1). BDB1 is an autosomal dominant skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In BDB1 the middle phalanges are short but in addition the terminal phalanges are rudimentary or absent. Both fingers and toes are affected. The thumbs and big toes are usually deformed. Defects in ROR2 are a cause of recessive Robinow syndrome (RRS). RRS is an autosomal disorder characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly and a dysmorphic facial appearance. The protein contains 1 frizzled (FZ) domain, 1 immunoglobulin-like C2-type domain, and 1 kringle domain.
Synonyms: Tyrosine-protein kinase transmembrane receptor ROR2, Neurotrophic tyrosine kinase, receptor-related 2 NTRKR2
Molecular Weight 104726 DA
Gene ID 4920
NCBI Accession NP_004551
Research Area Phospho-specific antibodies, Stem Cells, Cell Signaling, Protein Modifications, Cell Structure
Pathways RTK Signaling, WNT Signaling
Application Notes WB = 1:1000, IHC (p) = 1:10-50
Restrictions For Research Use only
Format Liquid
Concentration 2 mg/mL
Buffer PBS with 0.09 % (W/V) sodium azide
Preservative Sodium azide
Precaution of Use This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage 4 °C/-20 °C
Storage Comment Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
Expiry Date 6 months
Supplier Images
Western Blotting (WB) image for anti-ROR2 antibody (Receptor Tyrosine Kinase-Like Orphan Receptor 2) (ABIN392046) Western blot analysis of anti-ROR2 Antibody (ABIN392046) in K562 cell line lysates (3...
Immunohistochemistry (IHC) image for anti-ROR2 antibody (Receptor Tyrosine Kinase-Like Orphan Receptor 2) (ABIN392046) Formalin-fixed and paraffin-embedded human brain tissue reacted with ROR2 antibody, w...
Product cited in: Cerpa, Latorre-Esteves, Barria: "RoR2 functions as a noncanonical Wnt receptor that regulates NMDAR-mediated synaptic transmission." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 112, Issue 15, pp. 4797-802, 2015 (PubMed).

Background publications Schwabe, Tinschert, Buschow et al.: "Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B." in: American journal of human genetics, Vol. 67, Issue 4, pp. 822-31, 2000 (PubMed).

van Bokhoven, Celli, Kayserili et al.: "Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome." in: Nature genetics, Vol. 25, Issue 4, pp. 423-6, 2000 (PubMed).

Afzal, Rajab, Fenske et al.: "Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2." in: Nature genetics, Vol. 25, Issue 4, pp. 419-22, 2000 (PubMed).

Oldridge, Fortuna, Maringa et al.: "Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B." in: Nature genetics, Vol. 24, Issue 3, pp. 275-8, 2000 (PubMed).

Masiakowski, Carroll: "A novel family of cell surface receptors with tyrosine kinase-like domain." in: The Journal of biological chemistry, Vol. 267, Issue 36, pp. 26181-90, 1993 (PubMed).

Catalog No. ABIN392046
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