Key features and details
- Rabbit polyclonal to Liver Arginase (Biotin)
- Suitable for: WB, Dot blot, ELISA, Immunomicroscopy
- Reacts with: Cow
- Conjugation: Biotin
- Isotype: IgG
Product nameAnti-Liver Arginase antibody (Biotin)
See all Liver Arginase primary antibodies
DescriptionRabbit polyclonal to Liver Arginase (Biotin)
Tested applicationsSuitable for: WB, Dot blot, ELISA, Immunomicroscopymore details
Species reactivityReacts with: Cow
Tissue/ cell preparation liver Arginase (Bovine liver).
- Purified and partially purified Arginase [Bovine Liver]
10-20 Biotin molecules per rabbit IgG molecule.
Storage instructionsShipped at 4°C. Store at +4°C short term (1-2 weeks). Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Storage bufferpH: 7.20
Preservative: 0.01% Sodium azide
Constituents: 1% BSA, 0.42% Potassium phosphate, 0.87% Sodium chloride
BSA is IgG and Protease free
Concentration information loading...
Purification notesThis product is an IgG fraction antibody purified from monospecific antiserum by a multi-step process including delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against buffer.
Our Abpromise guarantee covers the use of ab34666 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ELISA: 1/1000 - 1/4000.
This antibody has been assayed against 1.0µg of liver Arginase in a standard capture ELISA using Peroxidase conjugated streptavidin and ABTS (2,2'-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) as a substrate for 30 minutes at RT.
IM: Use at an assay dependent dilution.
WB: Use at an assay dependent dilution. Predicted molecular weight: 36 kDa.
Suitable for other antibody based assays using streptavidin or avidin conjugates.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
PathwayNitrogen metabolism; urea cycle; L-ornithine and urea from L-arginine: step 1/1.
Involvement in diseaseDefects in ARG1 are the cause of argininemia (ARGIN) [MIM:207800]; also known as hyperargininemia. Argininemia is a rare autosomal recessive disorder of the urea cycle. Arginine is elevated in the blood and cerebrospinal fluid, and periodic hyperammonemia occurs. Clinical manifestations include developmental delay, seizures, mental retardation, hypotonia, ataxia, progressive spastic quadriplegia.
Sequence similaritiesBelongs to the arginase family.
- Information by UniProt
- A I antibody
- Al antibody
- ARG 1 antibody
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
ab34666 has not yet been referenced specifically in any publications.