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>   首页   >   产品   >   一抗   >   代谢   >   PNPLA2 Antibody (monoclonal) (M01)   

PNPLA2 Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a partial recombinant PNPLA2.

     
  • 1 - PNPLA2 Antibody (monoclonal) (M01) AT3363a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (36.74 KDa) .
  • 1 - PNPLA2 Antibody (monoclonal) (M01) AT3363a
    PNPLA2 monoclonal antibody (M01), clone 2H1. Western Blot analysis of PNPLA2 expression in PC-12.
  • 10 - PNPLA2 Antibody (monoclonal) (M01) AT3363a
    Detection limit for recombinant GST tagged PNPLA2 is approximately 3ng/ml as a capture antibody.
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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, E
Primary Accession Q96AD5
Other Accession NM_020376
Reactivity Human, Rat
Host mouse
Clonality monoclonal
Isotype IgG2a Kappa
Clone Names 2H1
Calculated MW 55316 Da
Additional Information
Gene ID 57104
Other Names Patatin-like phospholipase domain-containing protein 2, Adipose triglyceride lipase, Calcium-independent phospholipase A2, Desnutrin, IPLA2-zeta, Pigment epithelium-derived factor, TTS22, Transport-secretion protein 2, TTS2, PNPLA2, ATGL
Target/Specificity PNPLA2 (NP_065109, 347 a.a. ~ 446 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
E~~N/A
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsPNPLA2 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas

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

BACKGROUND

This gene encodes an enzyme which catalyzes the first step in the hydrolysis of triglycerides in adipose tissue. Mutations in this gene are associated with neutral lipid storage disease with myopathy.

REFERENCES

High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy. Lan MY, et al. Clin Genet, 2010 Mar 29. PMID 20370797.Rare ATGL haplotypes are associated with increased plasma triglyceride concentrations in the Greenland Inuit. Johansen CT, et al. Int J Circumpolar Health, 2010 Feb. PMID 20167152.Chronic TNFalpha and cAMP pre-treatment of human adipocytes alter HSL, ATGL and perilipin to regulate basal and stimulated lipolysis. B?zaire V, et al. FEBS Lett, 2009 Sep 17. PMID 19695247.Characterization of desnutrin functional domains: critical residues for triacylglycerol hydrolysis in cultured cells. Duncan RE, et al. J Lipid Res, 2010 Feb. PMID 19692632.Contribution of adipose triglyceride lipase and hormone-sensitive lipase to lipolysis in hMADS adipocytes. Bezaire V, et al. J Biol Chem, 2009 Jul 3. PMID 19433586.

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