Liver Arginase anticorps (AA 11-230)
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- Antigène Voir toutes Liver Arginase (ARG1) Anticorps
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
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Épitope
- AA 11-230
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Reactivité
- Humain
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Hôte
- Souris
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp Liver Arginase est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC)
- Purification
- Protein G Chromatography
- Immunogène
- A partial length recombinant Arginase-1 protein (amino acids 11-230) was used as the immunogen for this antibody
- Clone
- ABM4B35
- Isotype
- IgG2b kappa
- Top Product
- Discover our top product ARG1 Anticorps primaire
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- Indications d'application
- WB: 2-4 μg/mL, IHC: 5-15 μg/mL
- Restrictions
- For Research Use only
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- Concentration
- 0.5 mg/mL
- Buffer
- PBS containing 0.05 % BSA, PH 7.4
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.
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- Antigène
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
- Autre désignation
- Arginase-1 (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
- Arginase-1 (Arg-1) is a binuclear manganese metalloenzyme that catalyzes the hydrolysis of arginine to ornithine and urea. It is expressed in normal human liver with a high degree of specificity, concentrated in periportal hepatocytes. Arginase-1 are urea cycle enzymes used to distinguish hepatocellular carcinoma from other carcinomas. Two transcript variants encoding different isoforms have been found for this gene. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.
- Poids moléculaire
- 35 kDa
- ID gène
- 383
- UniProt
- P05089
- Pathways
- Cellular Response to Molecule of Bacterial Origin
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