Methylmalonic Aciduria Type A Protein, Mitochondrial (MMAA) Antibody

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Catalogue No: abx034519
Price: US$326.25
(Size: 80 µl)

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Datasheet SDS
The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria.

Target Methylmalonic Aciduria Type A Protein, Mitochondrial (MMAA)
Clonality Polyclonal
Reactivity Human, Mouse
Tested Applications ELISA, WB, IHC
Host Rabbit
Recommended dilutions WB: 1/1000, IHC-P: 1/50 - 1/100. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen KLH-conjugated synthetic peptide between 56-84 amino acids from the N-terminal region of human MMAA.
Isotype IgG
Form Liquid
Purification Purified through a protein A column, followed by peptide affinity purification.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC Q8IVH4 (UniProt, ExPASy)
UniProt Secondary AC B3KX40, Q495G7
UniProt Entry Name MMAA_HUMAN
Gene Symbol MMAA
KEGG hsa:166785
String 9606.ENSP00000281317
Molecular Weight Calculated MW: 46.5 kDa
Buffer PBS containing 0.09% sodium azide.
Availability Shipped within 5-10 working days.
Note This product is for research use only.
Research Articles on Methylmalonic Aciduria Type A Protein, Mitochondrial (MMAA)


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