Recombinant Human Methylmalonic Aciduria cblD type; with Homocystinuria
Product Sizes
20 µg
£528.00
32-4218-20UG
About this Product
- SKU:
- 32-4218
- Additional Names:
- Chromosome 2 Open Reading Frame 25||Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type With Homocystinuria||Methylmalonic Aciduria And Homocystinuria Type D Protein Mitochondrial||Protein C2orf25 Mitochondrial||CL25022||C2orf25||cblD.
- Extra Details:
- Source : Escherichia Coli. MMADHC Human Recombinant produced in E.coli is a single; non-glycosylated polypeptide chain containing 281 amino acids (39-296) and having a molecular mass of 31.0 kDa. MMADHC is fused to a 23 amino acid His-tag at N-terminus. MMADHC is a mitochondrial protein which takes part in an early step of vitamin B1 2 metabolism. Vitamin B12 (cobalamin) is vital for regular development and existence in humans. Mutations in MMADHC can result in methylmalonic aciduria and homocystinuria type cblD; a cobalamin metabolism syndrome which is characterized by decreased levels of the coenzymes methylcobalamin and adenosylcobalamin.
- Purification:
- Greater than 90% as determined by SDS-PAGE.
- Shipping Conditions:
- Blue Ice
- Storage Conditions:
- Store at 4[o]C if entire vial will be used within 2-4 weeks. Store; frozen at -20[o]C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).Avoid multiple freeze-thaw cycles.
- Supplier:
- Abeomics
- Type:
- Proteins, Peptides, Small Molecules & Other Biomolecules:Recombinant Proteins
- Manufacturer's Data Sheet:1.jpg
