Arginase, Liver (ARG1) Peptide
ARG1
Reactivity: Mammalian
Host: Synthetic
BP, IHC, WB
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- Target See all Liver Arginase (ARG1) products
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
- Peptide Type
- Synthetic
- Origin
- Mammalian
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
- Sequence
- LDIMEVNPSL GKTPEEVTRT VNTAVAITLA CFGLAREGNH KPIDYLNPPK
- 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
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Handling Advice
- Avoid repeated freeze/thaw cycles.
- Storage
- -20 °C
- Storage Comment
- Store at -20 °C long term.
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- Target
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
- Synonyms
- SI:zC146F4.4 (novel protein with NUDIX domain) Peptide, si:ch211-146f4.3 Peptide, argi1 Peptide, AI Peptide, AI256583 Peptide, Arg-1 Peptide, PGIF Peptide, arginase 1 Peptide, arginase Peptide, Arginase-1 Peptide, arginase, liver Peptide, L-arginase Peptide, arg1 Peptide, PGTG_16455 Peptide, argi1 Peptide, ARG1 Peptide, Arg1 Peptide
- 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.
- Molecular Weight
- 35 kDa
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