Arginase, Liver (ARG1) Peptide
ARG1
Reactivité: Mammifères
Hôte: Synthetic
BP, IHC, WB
N° du produit ABIN940233
Aperçu rapide pour Arginase, Liver (ARG1) Peptide (ABIN940233)
Antigène
Liver Arginase (ARG1)
(Arginase, Liver (ARG1))
Origine
Mammifères
Source
Synthetic
Application
Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
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Type de proteíne
- Synthetic
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Séquence
- LDIMEVNPSL GKTPEEVTRT VNTAVAITLA CFGLAREGNH KPIDYLNPPK
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Attributs du produit
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A synthetic peptide for use as a blocking control in assays to test for specificity of ARG1 antibody,
Alternative Names: Arginase 1 control peptide, Arginase 1 antibody Blocking Peptide, Anti-Arginase 1 Blocking Peptide, ARG Blocking Peptide, Liver Arginase Blocking Peptide, A I Blocking Peptide, Al Blocking Peptide, ARG 1 Blocking Peptide, ARG1 Blocking Peptide, Arginase 1 Blocking Peptide, Arginase liver Blocking Peptide, Arginase type I Blocking Peptide, Arginase1 Blocking Peptide, Liver type arginase Blocking Peptide, Type I arginase Blocking Peptide
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Indications d'application
- Optimal conditions should be determined by the investigator
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
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Buffer
- PBS
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Conseil sur la manipulation
- Avoid repeated freeze/thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20 °C long term.
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- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
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Sujet
- Arginase catalyzes the hydrolysis of arginine to ornithine and urea. The type I isoform of ARG1, 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.
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Poids moléculaire
- 35 kDa
Antigène
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