Arginase, Liver (ARG1) Peptide
ARG1
Reactivity: Mammalian
Host: Synthetic
BP, IHC, WB
Catalog No. ABIN940233
Quick Overview for Arginase, Liver (ARG1) Peptide (ABIN940233)
Target
Liver Arginase (ARG1)
(Arginase, Liver (ARG1))
Origin
Mammalian
Source
Synthetic
Application
Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
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Peptide Type
- Synthetic
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Sequence
- LDIMEVNPSL GKTPEEVTRT VNTAVAITLA CFGLAREGNH KPIDYLNPPK
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Characteristics
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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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Application Notes
- 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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Handling Advice
- Avoid repeated freeze/thaw cycles.
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Storage
- -20 °C
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Storage Comment
- Store at -20 °C long term.
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- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
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Background
- 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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Molecular Weight
- 35 kDa
Target
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