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          • Primary Antibodies ›
          • ROR2 Antibodies

          Fabgennix

          ROR2 Polyclonal Antibody, FITC

          View all (38) ROR2 antibodies
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          Datasheet
          Protocols
          Questions & Answers

          Cite ROR2 Polyclonal Antibody, FITC

          Product Details

          ROR2-FITC

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          1:500-1:1,000
          -

          Immunohistochemistry (IHC)

          1:50-1:250
          -

          ELISA (ELISA)

          1:10,000
          -

          Immunoprecipitation (IP)

          1:50-1:250
          -
          Product Specifications

          Species Reactivity

          Human, Mouse, Rat

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          Synthetic peptide taken within amino acid region 900-943 on human ROR2 protein.
          View immunogen

          Conjugate

          FITC FITC FITC

          Excitation/Emission Max

          498/517 nm View spectra spectra

          Form

          Liquid

          Concentration

          0.5-1.5 mg/mL

          Purification

          Affinity chromatography

          Storage buffer

          proprietary buffer, pH 7.4-7.8, with 0.5% BSA, 30% glycerol

          Contains

          0.02% sodium azide

          Storage conditions

          -20°C, store in dark

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          Target Information

          ROR2 (receptor tyrosine kinase-like orphan receptor 2) is a type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. It is thought to be involved in the early formation of the chondrocytes and 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.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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          Cite this product

          Bioinformatics

          Protein Aliases: neurotrophic tyrosine kinase receptor-related 2; neurotrophic tyrosine kinase, receptor related 2; Neurotrophic tyrosine kinase, receptor-related 2; receptor tyrosine kinase-like orphan receptor 2; Tyrosine-protein kinase transmembrane receptor ROR2

          View more View less

          Gene Aliases: BDB; BDB1; mRor2; NTRKR2; ROR2

          View more View less

          UniProt ID: (Human) Q01974

          View more View less

          Entrez Gene ID: (Human) 4920, (Rat) 306782, (Mouse) 26564

          View more View less

          Function(s)
          transmembrane receptor protein tyrosine kinase activity frizzled binding protein binding ATP binding Wnt-protein binding metal ion binding coreceptor activity involved in Wnt signaling pathway, planar cell polarity pathway nucleotide binding protein kinase activity protein tyrosine kinase activity kinase activity transferase activity transferase activity, transferring phosphorus-containing groups
          Process(es)
          cartilage condensation somitogenesis signal transduction transmembrane receptor protein tyrosine kinase signaling pathway Wnt signaling pathway, calcium modulating pathway smoothened signaling pathway JNK cascade multicellular organism development negative regulation of cell proliferation peptidyl-tyrosine phosphorylation positive regulation of cell migration BMP signaling pathway embryonic genitalia morphogenesis inner ear morphogenesis embryonic digit morphogenesis cell fate commitment positive regulation of transcription, DNA-templated Wnt signaling pathway, planar cell polarity pathway SMAD protein signal transduction negative regulation of canonical Wnt signaling pathway positive regulation of canonical Wnt signaling pathway skeletal system development cell differentiation regulation of canonical Wnt signaling pathway protein phosphorylation phosphorylation
          It has to be done as per old AB suggested Products section.
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