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>   首页   >   产品   >   一抗   >   癌症   >   ARHGAP20 antibody - middle region   

ARHGAP20 antibody - middle region

Rabbit Polyclonal Antibody

     
  • 1 - ARHGAP20 antibody - middle region AI14124

    WB Suggested Anti-ARHGAP20 Antibody Titration: 0.2-1 μg/ml
    ELISA Titer: 1:1562500
    Positive Control: 721_B cell lysate
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB
Primary Accession Q9P2F6
Other Accession NM_020809, NP_065860
Reactivity Human, Mouse, Rat, Rabbit, Pig, Dog, Guinea Pig, Horse, Bovine
Predicted Mouse, Rabbit, Pig, Dog, Guinea Pig, Horse, Bovine
Host Rabbit
Clonality Polyclonal
Calculated MW 132608 Da
Additional Information
Gene ID 57569
Alias Symbol KIAA1391, RARHOGAP
Other Names Rho GTPase-activating protein 20, Rho-type GTPase-activating protein 20, ARHGAP20, KIAA1391
Format Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Reconstitution & Storage Add 50 ul of distilled water. Final anti-ARHGAP20 antibody concentration is 1 mg/ml in PBS buffer with 2% sucrose. For longer periods of storage, store at 20°C. Avoid repeat freeze-thaw cycles.
PrecautionsARHGAP20 antibody - middle region is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name ARHGAP20
Synonyms KIAA1391
Function GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state.
Tissue Location Expressed predominantly in the brain. Lower expression is found in lymph nodes.
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

REFERENCES

Kalla C.,et al.Genes Chromosomes Cancer 42:128-143(2005).
Nagase T.,et al.DNA Res. 7:65-73(2000).
Mural R.J.,et al.Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases.
Ota T.,et al.Nat. Genet. 36:40-45(2004).
Katoh M.,et al.Int. J. Oncol. 23:1471-1476(2003).

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