alpha-Methylacyl-CoA Racemase (AMACR) Peptide
AMACR
Reactivity: Mammalian
Host: Synthetic
BP, WB, IHC
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- Target See all AMACR products
- AMACR (alpha-Methylacyl-CoA Racemase (AMACR))
- Peptide Type
- Synthetic
- Origin
- Mammalian
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- IFDGTDACVT PVLTFEEVVH HDHNKERGSF ITSEEQDVSP RPAPLLLNTP
- Characteristics
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A synthetic peptide for use as a blocking control in assays to test for specificity of AMACR antibody,
Alternative Names: AMACR control peptide, AMACR antibody Blocking Peptide, Anti-AMACR Blocking Peptide, alpha-methylacyl-CoA racemase Blocking Peptide, CBAS4 Blocking Peptide, RACE Blocking Peptide, RM 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
- AMACR (alpha-Methylacyl-CoA Racemase (AMACR))
- Synonyms
- AMACR Peptide, DKFZp469O1232 Peptide, amacr Peptide, NCU04099.1 Peptide, MGC89832 Peptide, AMACRD Peptide, CBAS4 Peptide, RACE Peptide, RM Peptide, Macr1 Peptide, Da1-8 Peptide, Marc1 Peptide, alpha-methylacyl-CoA racemase Peptide, PROBABLE ALPHA-METHYLACYL-COA RACEMASE MCR (2-methylacyl-CoA racemase) (2-arylpropionyl-CoA epimerase) Peptide, Alpha-methylacyl-CoA racemase Peptide, alpha-methylacyl-CoA racemase L homeolog Peptide, AMACR Peptide, mcr Peptide, BPSL0064 Peptide, Maqu_2037 Peptide, UREG_03852 Peptide, MCYG_01809 Peptide, amacr Peptide, amacr.L Peptide, MGYG_04259 Peptide, NCU04099 Peptide, Amacr Peptide
- Background
- This gene encodes a racemase. The encoded enzyme interconverts pristanoyl-CoA and C27-bile acylCoAs between their (R)- and (S)-stereoisomers. The conversion to the (S)-stereoisomers is necessary for degradation of these substrates by peroxisomal beta-oxidation. Encoded proteins from this locus localize to both mitochondria and peroxisomes. Mutations in this gene may be associated with adult-onset sensorimotor neuropathy, pigmentary retinopathy, and adrenomyeloneuropathy due to defects in bile acid synthesis. Alternatively spliced transcript variants have been described. Read-through transcription also exists between this gene and the upstream neighboring C1QTNF3 (C1q and tumor necrosis factor related protein 3) gene.
- Molecular Weight
- 42 kDa
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