Liver Arginase anticorps (AA 1-292)
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- Antigène Voir toutes Liver Arginase (ARG1) Anticorps
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
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Épitope
- AA 1-292
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Liver Arginase est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
- Purification
- Purified by antigen-affinity chromatography.
- Immunogène
- Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 292 of arginase I
- Top Product
- Discover our top product ARG1 Anticorps primaire
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- Indications d'application
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Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.500
Immunofluorescence: 1.100-1.200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
- Agent conservateur
- Thimerosal (Merthiolate)
- Précaution d'utilisation
- Biohazard Informations: This product contains thimerosal which is hazardous.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- Antigène
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
- Autre désignation
- arginase I (ARG1 Produits)
- Synonymes
- anticorps SI:zC146F4.4 (novel protein with NUDIX domain), anticorps si:ch211-146f4.3, anticorps argi1, anticorps AI, anticorps AI256583, anticorps Arg-1, anticorps PGIF, anticorps arginase 1, anticorps arginase, anticorps Arginase-1, anticorps arginase, liver, anticorps L-arginase, anticorps arg1, anticorps PGTG_16455, anticorps argi1, anticorps ARG1, anticorps Arg1
- Sujet
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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 encoded by this gene, 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.[provided by RefSeq]
- Poids moléculaire
- 35 kDa
- ID gène
- 383
- NCBI Accession
- NM_000045, NP_000036
- Pathways
- Cellular Response to Molecule of Bacterial Origin
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