Liver Arginase antibody (C-Term)
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- Target See all Liver Arginase (ARG1) Antibodies
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
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Binding Specificity
- C-Term
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Reactivity
- Rat, Mouse
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Host
- Goat
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Clonality
- Polyclonal
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Conjugate
- This Liver Arginase antibody is un-conjugated
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Application
- Western Blotting (WB)
- Sequence
- C-NHKPETDYLK PPK
- Specificity
- This antibody detects Arginase-1.
- Cross-Reactivity (Details)
- Species reactivity (tested):Mouse, Rat.
- Purification
- Ammonium Sulphate Precipitation followed by Antigen Affinity Chromatography using the immunizing peptide
- Immunogen
- Peptide from the C-Terminus of the protein sequence according to NP_058830.2 Genename: Arg1
- Top Product
- Discover our top product ARG1 Primary Antibody
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- Application Notes
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Peptide ELISA: antibody detection limit dilution 1: 32000. Western blot: 0.01-0.03 μg/mL. Approx 37 kDa band observed in Mouse Liver and Rat Liverlysates (calculated MW of 35.7 kDa according to NP_058830.1).
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. - Restrictions
- For Research Use only
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- Concentration
- 0.5 mg/mL
- Buffer
- Tris saline, pH ~7.3, 0.02 % Sodium Azide, 0.5 % BSA
- Preservative
- Sodium azide
- Precaution of Use
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handling Advice
- Avoid repeated freezing and thawing.
- Storage
- 4 °C/-20 °C
- Storage Comment
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Target
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
- Alternative Name
- Arginase-1 (ARG1 Products)
- 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: ARG1, Liver-type arginase, Type I arginase
- Gene ID
- 11846, 10090
- UniProt
- Q61176
- Pathways
- Cellular Response to Molecule of Bacterial Origin
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