MMAA 产品
(Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
Categories
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].
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Featured MMAA Categories
Recommended MMAA 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human, Mouse
Application
WB, IHC (p)
Validations
- (3)
Cat. No.
ABIN653752
Quantity
400 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
- (1)
Cat. No.
ABIN531168
Quantity
50 μg
Datasheet
Datasheet
Reactivity
Human, Mouse, Rat
Application
WB, IF (p), IHC (p)
Validations
Cat. No.
ABIN1387231
Quantity
100 μL
Datasheet
Datasheet
Recommended MMAA 蛋白
Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Source
Wheat germ
Validations
- (1)
Cat. No.
ABIN1802257
Quantity
10 μg
Datasheet
Datasheet
Reactivity
Human
Source
Wheat germ
Validations
- (1)
Cat. No.
ABIN1311037
Quantity
25 μg
Datasheet
Datasheet
Reactivity
Human
Source
HEK-293 Cells
Validations
- (1)
Cat. No.
ABIN2726115
Quantity
20 μg
Datasheet
Datasheet
Latest Publications for our MMAA Products
: "Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation." in: The Journal of biological chemistry, Vol. 285, Issue 49, pp. 38204-13, (2010) (PubMed).Synonyms and alternative names related to MMAA
methylmalonic aciduria (cobalamin deficiency) type A (Mmaa), methylmalonic aciduria (cobalamin deficiency) cblA type (MMAA), methylmalonic aciduria (cobalamin deficiency) cblA type (Mmaa), 2810018E08Rik, AI840684, cblAProtein level used designations for MMAA
- methylmalonic aciduria type A homolog, mitochondrial
- methylmalonic aciduria type A protein, mitochondrial
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