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>   首页   >   产品   >   一抗   >   代谢   >   ASAH1 Antibody (monoclonal) (M01)   

ASAH1 Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a partial recombinant ASAH1.

     
  • 1 - ASAH1 Antibody (monoclonal) (M01) AT1207a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (36.74 KDa) .
  • 2 - ASAH1 Antibody (monoclonal) (M01) AT1207a
    Immunoperoxidase of monoclonal antibody to ASAH1 on formalin-fixed paraffin-embedded human heart. [antibody concentration 3 ug/ml]
  • 10 - ASAH1 Antibody (monoclonal) (M01) AT1207a
    Detection limit for recombinant GST tagged ASAH1 is 0.1 ng/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, IHC, E
Primary Accession Q13510
Other Accession NM_177924
Reactivity Human
Host mouse
Clonality monoclonal
Isotype IgG3 Kappa
Clone Names 2C9
Calculated MW 44660 Da
Additional Information
Gene ID 427
Other Names Acid ceramidase, AC, ACDase, Acid CDase, Acylsphingosine deacylase, N-acylsphingosine amidohydrolase, Putative 32 kDa heart protein, PHP32, Acid ceramidase subunit alpha, Acid ceramidase subunit beta, ASAH1, ASAH
Target/Specificity ASAH1 (NP_808592, 25 a.a. ~ 124 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
IHC~~1:100~500
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.
PrecautionsASAH1 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 a heterodimeric protein consisting of a nonglycosylated alpha subunit and a glycosylated beta subunit that is cleaved to the mature enzyme posttranslationally. The encoded protein catalyzes the synthesis and degradation of ceramide into sphingosine and fatty acid. Mutations in this gene have been associated with a lysosomal storage disorder known as Farber disease. Multiple transcript variants encoding several distinct isoforms have been identified for this gene.

REFERENCES

1.Ceramide biosynthesis and metabolism in trophoblast syncytialization.Singh AT, Dharmarajan A, Aye IL, Keelan JA.Mol Cell Endocrinol. 2012 May 28.

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