Liver Arginase anticorps (Arg1, C-Term)
Aperçu rapide pour Liver Arginase anticorps (Arg1, C-Term) (ABIN374811)
Antigène
Voir toutes Liver Arginase (ARG1) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- Arg1, C-Term
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Séquence
- C-REGNHKPIDY LNPPK
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Specificité
- This antibody detects Arginase-1.
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Réactivité croisée (Details)
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Species reactivity (expected):Canine (Dog).
Species reactivity (tested):Human. -
Purification
- Ammonium Sulphate Precipitation followed by Antigen Affinity Chromatography using the immunizing peptide
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Immunogène
- Peptide from the C Terminus of the protein sequence according to NP_000036.2 Genename: ARG1
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Indications d'application
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Peptide ELISA: antibody detection limit dilution 1: 2000. Western blot: 0.03-0.1 μg/mL. Approx 35 kDa band observed in Human Liver lysates(calculated MW of 34.5 kDa according to NP_000036.2. Additional bands of unknown identity were also consistently observed at 19-25 kDa. Thiesebands were successfully blocked by incubation with the immunising peptide. We wouldappreciate any feedback from people in the field - have any such results been reportedwith other antibodies/lysates? Have any further splice variants/modified forms beenreported?
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
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Buffer
- Tris saline, pH ~7.3 containing 0.02 % Sodium Azide as preservative and 0.5 % BSA as stabilizer
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- Avoid repeated freezing and thawing.
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Stock
- 4 °C/-20 °C
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Stockage commentaire
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
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Autre désignation
- Arginase-1
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Sujet
- 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
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ID gène
- 383, 9606
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UniProt
- P05089
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Pathways
- Cellular Response to Molecule of Bacterial Origin
Antigène
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