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Rabbit anti-Human ROR2 Polyclonal Antibody

The antibody against ROR2 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 100-200 of human ROR2 (NP_004551.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

ADA-11191A

The antibody against ROR2 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 100-200 of human ROR2 (NP_004551.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

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Specifications


Cat.No ADA-11191A ClonalityPolyclonal
Host SpeciesRabbitTarget NameROR2
Target SynonymsBDB; BDB1; NTRKR2; ROR2FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesMouse embryoApplicationELISA, WB, IHC-P

Immunogen Information


Immunogen DescriptionA synthetic peptide corresponding to a sequence within amino acids 100-200 of human ROR2 (NP_004551.2).Target SpeciesHuman
Immunogen SequenceAPVVQEPRRIIIRKTEYGSRLRIQDLDTTDTGYYQCVATNGMKTITATGVLFVRLGPTHSPNHNFQDDYHEDGFCQPYRGIACARFIGNRTIYVDSLQMQGUniprot IDQ01974
Background Information
  • Uniprot Id

    Q01974

  • Target Species

    Human

  • Target Name

    ROR2

  • Target Full Name

    Tyrosine-protein kinase transmembrane receptor ROR2

  • Target Function

    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. Phosphorylates YWHAB, leading to induction of osteogenesis and bone formation. In contrast, has also been shown to have very little tyrosine kinase activity in vitro. May act as a receptor for wnt ligand WNT5A which may result in the inhibition of WNT3A-mediated signaling.

  • Target Involvement

    Brachydactyly B1 (BDB1); Robinow syndrome autosomal recessive (RRS)

  • Target Subcellular Location

    Cell membrane; Single-pass type I membrane protein.

  • Target Protein Families

    Protein kinase superfamily, Tyr protein kinase family, ROR subfamily

  • Target Synonyms

    BDB; BDB1; NTRKR2; ROR2

  • Target 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.

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