Metabolism Antibodies 2

ROR2 Rabbit Polyclonal Antibody (CAB5620)

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SKU:
CAB5620
Product Type:
Antibody
Host Species:
Rabbit
Isotype:
IgG
Antibody Type:
Polyclonal Antibody
Research Area:
Metabolism
Reactivity:
Human, Mouse, Rat
Synonyms:
BDB, BDB1, NTRKR2, ROR2
Research Use:
Metabolism
Frequently bought together:

Description

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ROR2 Antibody (CAB5620)

The ROR2 Antibody (CAB5620) is a high-quality antibody developed for reliable detection and analysis of target proteins. This antibody, raised in rabbits, is highly specific to human samples and is validated for use in Western blot applications. By binding to the ROR2 protein, this antibody enables the detection and analysis of ROR2 in a variety of cell types.The ROR2 protein is known to play a crucial role in various biological processes, including skeletal development, cell migration, and tissue regeneration. Dysregulation of ROR2 has been linked to developmental disorders and certain types of cancer, making it a promising target for therapeutic interventions.

This antibody is validated for use in WB, ELISA applications and has demonstrated reactivity against Human, Mouse, Rat samples.

Product Name:ROR2 Antibody
SKU:CAB5620
Size:20μL, 100μL
Reactivity:Human, Mouse, Rat
Conjugate:Unconjugated
Immunogen:Synthetic peptide. This information is considered to be commercially sensitive.
Sequence:APVV QEPR RIII RKTE YGSR LRIQ DLDT TDTG YYQC VATN GMKT ITAT GVLF VRLG PTHS PNHN FQDD YHED GFCQ PYRG IACA RFIG NRTI YVDS LQMQ G
Tested Applications:WB ELISA
Recommended Dilution:
WB1:500 - 1:1000
ELISARecommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Synonyms:BDB, BDB1, NTRKR2, ROR2
Positive Sample:Mouse embryo
Cellular Localization:Cell Membrane, Single-Pass Type I Membrane Protein.
Calculated MW:105kDa
Observed MW:140kDa

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.

Purification MethodAffinity purification
Gene ID4920
RRIDAB_2766381
Buffer InformationStore at -20℃. Avoid freeze / thaw cycles. Buffer: PBS containing 50% glycerol, preserved with proclin300 or sodium azide, pH 7.3.
Product ImageWestern blot analysis of lysates from Mouse embryo, using ROR2 Rabbit pAb (CAB5620) at 1:700 dilution. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (AbGn00020). Exposure time: 180s.
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