ARG1 Rabbit Polyclonal Antibody

Référence R1057A

Conditionnement : 10mg


ARG1 Rabbit Polyclonal Antibody

Be the first to review this product
SKU
R1057A
ARG1 rabbit polyclonal antibody, Azide Free
 
Specifications
Product Data
Application ELISA, ID, IF, IP, R, WB
Recommended Dilution This product is intended for use in precipitating and non-precipitating antibody-binding assays (such as e.g., ELISA and Western blotting and Immunofluorescence or Histochemical techniques), to prepare an insoluble immuno-affinity adsorbent, for labelling with a marker of choice.
Recommended Dilutions:
Non-precipitating antibody-binding techniques: 1/10-1/70.
Reactivity Bovine
Antibody Host Rabbit
Isotype IgG
Clonality Polyclonal
Immunogen Arginase isolated and purified from Calf liver.
Freund's complete adjuvant is used in the first step of the immunization procedure.
Specificity Arginase from Calf Liver.
The reagents were evaluated for potency, purity and specificity using most or all of the following techniques: Immunoelectrophoresis, Cross-Immunoelectrophoresis, Single Radial Immunodiffusion (Ouchterlony), block titration, ELISA, Immunoblotting and Enzyme Inhibition.
Cross-reactivity Cross-reactivities against enzymes of other sources may occur but have not been determined.
Buffer PBS, pH 7.2 without preservatives and foreign proteins
State: Azide Free
State: Lyophilized hyperimmune IgG fraction
Reconstitution Method Restore by adding 1 ml of sterile distilled water
Concentration lot specific
Purification Ammonium Sulphate Precipitation and Ion Exchange Chromatography
Conjugation Unconjugated
Storage Store the antibody lyophilized at 2-8°C and reconstituted at 2-8°C for one week or (in aliquots) at -20°C for longer.
If a slight precipitation occurs upon storage, this should be removed by centrifugation.
Stability Shelf life: one year from despatch.
Shipping Ambient
Database Link
Background 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 crossreactivity 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.
Synonyms Type I arginase, Liver-type arginase, ARG1
Reference Data

file-alt Citations

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Related Products