liver Arginase Antibody

liver Arginase Antibody

Product Information

Product Overview:

Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic cross reactivity and physiologic function. The type I isoform, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.

Application:

For IHC: Use suggested antigen retrieval using heat mediated 10mM Citrate buffer (pH6.0) or Tris-EDTA buffer (pH8.0).

Catalog#: NBP1-32731
LID#: 171617A
Quantity :
Order by Phone or Fax: 1.800.316.3081

Specifications

Host SpeciesRabbit
SpeciesHuman, Mouse
ControlsHepG2 cell line and mouse liver
Entrez Human ID383
LocalizationCytoplasm
Preservation0.01% Thimerosal
Species ReactivityHuman and Mouse.
Swissprot Human IDP05089
Gene SymbolARG1
ApplicationsWB, ICC/IF, IHC, IHC-P
Species AbbreviationHu, Mu
Grade/PurityImmunogen affinity purified
ClonalityPolyclonal
ImmunogenRecombinant fragment corresponding to a region within amino acids 1 and 322 of Arginase.
Storage Buffer1XPBS, 20% Glycerol (pH7).
DilutionImmunocytochemistry/Immunofluorescence 1:100-1:1000, Immunohistochemistry 1:100-1:1000, Immunohistochemistry-Paraffin 1:100-1:1000, Western Blot 1:1000-1:50000
Gene ID5973
Unit Size0.1mg
Concentration1.0 mg/ml
Safety StatementsThis product is for research use only and is not approved for use in humans or in clinical diagnosis.
Sample AvailabilityYes
Synonymarginase 1, arginase, liver, arginase-1, EC 3.5.3.1, Liver-type arginase, Type I arginase

Shipping & Handling

Estimated Ship Time: 3 Business Days

Shipped In: Blue Ice

Hazardous Material: No

Storage

Storage Temperature: Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.

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