MMAA (NM_172250) Human Mass Spec Standard

CAT#: PH323205

MMAA MS Standard C13 and N15-labeled recombinant protein (NP_758454)



  View other "MMAA" proteins (3)

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CNY 19,520.00


货期*
4周

规格
    • 10 ug

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经常一起买 (2)
Transient overexpression lysate of methylmalonic aciduria (cobalamin deficiency) cblA type (MMAA), nuclear gene encoding mitochondrial protein
    • 100 ug

CNY 4,840.00


MMAA mouse monoclonal antibody, clone OTI3G5 (formerly 3G5)
    • 100 ul

CNY 1,999.00
CNY 2,700.00

Specifications

Product Data
Description MMAA MS Standard C13 and N15-labeled recombinant protein (NP_758454)
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC223205
Predicted MW 39 kDa
Protein Sequence
Tag C-Myc/DDK
Purity > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration >0.05 µg/µL as determined by microplate BCA method
Labeling Method Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Buffer 25 mM Tris-HCl, 100 mM glycine, pH 7.3
Reference Data
RefSeq NP_758454
RefSeq Size 1473
RefSeq ORF 1254
Synonyms cblA
Locus ID 166785
Cytogenetics 4q31.21
Summary 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. [provided by RefSeq, Jul 2008]
Protein Families Druggable Genome
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