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MMAA Antibody

Novus Biologicals, part of Bio-Techne | Catalog # NBP2-97305

Novus Biologicals, part of Bio-Techne
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NBP2-97305-50ul
NBP2-97305-100ul

Key Product Details

Species Reactivity

Validated:

Human

Applications

Immunohistochemistry-Paraffin

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Product Summary for MMAA Antibody

Immunogen

Produced in rabbits immunized with E. coli-derived Human MMAA fragment.

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Description

This antibody can be stored at 2C to 8C for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20C to -80C. Avoid repeated freeze-thaw cycles.

Scientific Data Images for MMAA Antibody

Immunohistochemistry-Paraffin: MMAA Antibody [NBP2-97305]

Immunohistochemistry-Paraffin: MMAA Antibody [NBP2-97305]

Immunohistochemistry-Paraffin: MMAA Antibody [NBP2-97305] - Immunochemical staining of human MMAA in human liver with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.

Applications for MMAA Antibody

Application
Recommended Usage

Immunohistochemistry-Paraffin

1:50-1:200
Please Note: Optimal dilutions of this antibody should be experimentally determined.

Formulation, Preparation, and Storage

Purification

Antigen and protein A Affinity-purified

Formulation

PBS

Preservative

0.03% Proclin 300

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.

Background: MMAA

MMAA is 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]

Alternate Names

cblA, EC 3.6, methylmalonic aciduria (cobalamin deficiency) cblA type, methylmalonic aciduria (cobalamin deficiency) type A, MGC120011, MGC120012, MGC120013, mitochondrial

Gene Symbol

MMAA

Additional MMAA Products

Product Documents for MMAA Antibody

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Product Specific Notices for MMAA Antibody

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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