MMAA antibody (N-Term)
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- Target See all MMAA Antibodies
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
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Binding Specificity
- N-Term
- Reactivity
- Human, Rat, Horse, Rabbit, Cow, Dog, Guinea Pig
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This MMAA antibody is un-conjugated
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Application
- Western Blotting (WB)
- Sequence
- GQRACLAEAI TLVESTHSRK KELAQVLLQK VLLYHREQEQ SNKGKPLAFR
- Predicted Reactivity
- Cow: 85%, Dog: 86%, Guinea Pig: 92%, Horse: 86%, Human: 100%, Rabbit: 93%, Rat: 92%
- Characteristics
- This is a rabbit polyclonal antibody against MMAA. It was validated on Western Blot.
- Purification
- Affinity Purified
- Top Product
- Discover our top product MMAA Primary Antibody
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- Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
- Comment
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Antigen size: 418 AA
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Target
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
- Alternative Name
- MMAA (MMAA Products)
- Synonyms
- 2810018E08Rik antibody, AI840684 antibody, cblA antibody, methylmalonic aciduria (cobalamin deficiency) type A antibody, methylmalonic aciduria (cobalamin deficiency) cblA type antibody, Mmaa antibody, MMAA antibody
- Background
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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.
Alias Symbols: MGC120010, MGC120011, MGC120012, MGC120013, cblA
Protein Interaction Partner: MMAA, MUT,
Protein Size: 418 - Molecular Weight
- 46 kDa
- Gene ID
- 166785
- NCBI Accession
- NM_172250, NP_758454
- UniProt
- Q8IVH4
- Pathways
- Monocarboxylic Acid Catabolic Process
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