MMAA antibody (Methylmalonic Aciduria (Cobalamin Deficiency) Type A) (AA 56-84) Primary Antibody
MMAA
Reactivity: Human, Mouse
IHC (p), WB
Host: Rabbit
Polyclonal
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Catalog No. ABIN5538833
$570.63
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400 μL
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- Target
- Binding Specificity
- AA 56-84, N-Term
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Clonality
- Polyclonal
- Conjugate
- This MMAA antibody is un-conjugated
- Application
- Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogen
- This MMAA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-84 amino acids from the N-terminal region of human MMAA.
- Isotype
- Ig Fraction
-
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- Application Notes
- For WB starting dilution is: 1:500
For IHC-P starting dilution is: 1:50~100 - Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Supplied in PBS with 0.09 % (W/V) sodium azide.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- 4 °C,-20 °C
- Storage Comment
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
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- Target
- Alternative Name
- MMAA (MMAA Antibody Abstract)
- Background
- 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.
- Molecular Weight
- 47 kDa
- Gene ID
- 166785
- UniProt
- Q8IVH4
- Pathways
- Monocarboxylic Acid Catabolic Process
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