Mouse Monoclonal Anti-AMACR antibody (STJ99109)

$99.00$319.00

Reactivity: Rat
Applications: WB, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Mouse Monoclonal Anti-AMACR antibody (STJ99109)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, ELISA

Recommended dilution: WB 1:500-2000; ELISA 1:10000-20000

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody

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|2 methylacyl CoA racemase antibody|2-methylacyl-CoA racemase antibody|Alpha methylacyl CoA racemase antibody|Alpha-methylacyl-CoA racemase antibody|Amacr antibody|AMACR_HUMAN antibody|AMACRD antibody|CBAS4 antibody|EC 5.1.99.4 antibody|Macr1 antibody|RACE antibody|RM antibody|Anti-AMCR antibody (ab175280)
SCBT cat No: sc-136022|sc-81710|sc-514408|sc-514424|

Name

Anti-AMACR antibody

Catalogue No.

STJ99109

Reactivity

Rat

Specificity

Anti-AMACR antibody detects endogenous levels of AMACR (C-term) and does not cross-react with related proteins.

Immunogen

Purified recombinant human AMACR (C-term) protein fragments expressed in E.coli.

Host

Mouse

Applications

WB, ELISA

Recommended dilution

WB 1:500-2000; ELISA 1:10000-20000

Clonality

Monoclonal

Conjugation

Unconjugated

Isotype

IgG1

Molecular weight

42kDa

Formulation

Anti-AMACR antibody was tube-contained in liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Concentration

1 mg/ml

Purification

Anti-AMACR antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Storage

-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

2 methylacyl CoA racemase antibody, 2-methylacyl-CoA racemase antibody, Alpha methylacyl CoA racemase antibody, Alpha-methylacyl-CoA racemase antibody, Amacr antibody, AMACR_HUMAN antibody, AMACRD antibody, CBAS4 antibody, EC 5.1.99.4 antibody, Macr1 antibody, RACE antibody, RM antibody

Database links

UniProt/Swiss-Prot:Q9UHK6

Protein function

Racemization of 2-methyl-branched fatty acid CoA esters. Responsible for the conversion of pristanoyl-CoA and C27-bile acyl-CoAs to their (S)-stereoisomers.

Involvement in disease

Alpha-methylacyl-CoA racemase deficiency (AMACRD) [MIM:614307]: A rare autosomal recessive peroxisomal disorder characterized by elevated plasma concentrations of pristanic acid C27-bile-acid intermediates, and adult onset of variable neurodegenerative symptoms affecting the central and peripheral nervous systems. Features may include seizures, visual failure, sensorimotor neuropathy, spasticity, migraine, and white matter hyperintensities on brain imaging. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Congenital bile acid synthesis defect 4 (CBAS4) [MIM:214950]: A disorder characterized by the presence of trihydroxycoprostanic acid in the bile and absence of cholic acid. Patients manifest neonatal jaundice, intrahepatic cholestasis and bile duct deficiency. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the CaiB/BaiF CoA-transferase family.

Protein cellular localization

Peroxisome . Mitochondrion .

Research area

All research areas>Signaling Intermediates>P504S
(View all antibody categories related to Signaling Intermediates)

Note

AntibodyPlus can customize Anti-AMACR antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provide antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

St John’s Laboratory Ltd.

Product type

Primary antibody

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