NSJ Bioreagents

ROR2 Antibody

Product Code:
 
NSJ-F54941
Product Group:
 
Primary Antibodies
Supplier:
 
NSJ Bioreagents
Host Type:
 
Rabbit
Antibody Isotype:
 
Rabbit Ig
Antibody Clonality:
 
Polyclonal
Regulatory Status:
 
RUO
Target Species:
 
Human
Applications:
  • Immunohistochemistry- Paraffin Embedded (IHC-P)
  • Western Blot (WB)
Storage:
 
Aliquot the ROR2 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
1 / 4
Western blot testing of human 1) HeLa, 2) K562, 3) NCCIT, 4) SH-SY5Y and 5) T-47D cell lysate with ROR2 antibody. Expected molecular weight: 105-130 kDa.
2 / 4
Western blot testing of human 1) HeLa, 2) K562, 3) T-47D and 4) mouse NIH 3T3 cell lysate with ROR2 antibody. Expected molecular weight: 105-130 kDa.
3 / 4
Western blot testing of 1) non-transfected and 2) transfected 293 cell lysate with ROR2 antibody.
4 / 4
IHC testing of FFPE human cancer tissue with ROR2 antibody. HIER: steam section in pH6 citrate buffer for 20 min and allow to cool prior to staining.
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Western blot testing of human 1) HeLa, 2) K562, 3) NCCIT, 4) SH-SY5Y and 5) T-47D cell lysate with ROR2 antibody. Expected molecular weight: 105-130 kDa.
Western blot testing of human 1) HeLa, 2) K562, 3) T-47D and 4) mouse NIH 3T3 cell lysate with ROR2 antibody. Expected molecular weight: 105-130 kDa.
Western blot testing of 1) non-transfected and 2) transfected 293 cell lysate with ROR2 antibody.
IHC testing of FFPE human cancer tissue with ROR2 antibody. HIER: steam section in pH6 citrate buffer for 20 min and allow to cool prior to staining.

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CodeSizePrice
NSJ-F54941-0.08ML0.08 ml£260.00
Quantity:
NSJ-F54941-0.4ML0.4 ml£502.00
Quantity:
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Further Information

Application Details :
Immunohistochemistry (FFPE): 1:50-1:100, Western blot: 1:500-1:1000
Description:
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.
Format :
Purified
Formulation :
In 1X PBS, pH 7.4, with 0.09% sodium azide
Immunogen:
A portion of amino acids 915-943 from the human protein was used as the immunogen for the ROR2 antibody.
Limitation:
This ROR2 antibody is available for research use only.
Purity:
Purified
Species Reactivity :
Human
Uniprot #:
Q01974