MMADHC monoclonal antibody MB64001
Specifications
| 50ul/100ul |
Background:
This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X. [provided by RefSeq, Nov
Specificity:
methylmalonic aciduria and homocystinuria, cblD type
Alternative names:
C2orf25; cblD; CL25022
Species reactivity:
Human, Mouse, Rat
Host:
Mouse
Ig type:
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Immunogen:
Human recombinant protein fragment corresponding to amino acids 39-296 of human MMADHC (NP_056517) produced in E.coli.
Purification & Purity:
Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Molecular weight:
32.8 kDa(Predicted)
Applications:
WB
Usage:
WB 1:2000
Storage:
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Precautions:
For research use only, not for use in diagnostic procedure.
More info:
Email: info@sobekbio.com
Orders:
Email: orders@sobekbio.com
