MMADHC Antibody - BSA Free

Novus Biologicals | Catalog # NBP3-47083

Novus Biologicals
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Key Product Details

Species Reactivity

Human

Applications

Immunohistochemistry, Western Blot, ELISA

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Format

BSA Free
View all MMADHC Primary Antibodies »

Product Specifications

Immunogen

methylmalonic aciduria(cobalamin deficiency) cblD type, with homocystinuria. (Uniprot# Q9H3L0)

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Theoretical MW

33 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Scientific Data Images for MMADHC Antibody - BSA Free

MMADHC Antibody - BSA Free

Western Blot: MMADHC Antibody - BSA Free [NBP3-47083] -

Western Blot: MMADHC Antibody - BSA Free [NBP3-47083] - HeLa cells were subjected to SDS PAGE followed by western blot with (MMADHC Antibody) at dilution of 1:600
MMADHC Antibody - BSA Free

Immunohistochemistry: MMADHC Antibody - BSA Free [NBP3-47083] -

Immunohistochemistry: MMADHC Antibody - BSA Free [NBP3-47083] - Immunohistochemistry of paraffin-embedded human skeletal muscle tissue slide using (MMADHC Antibody) at dilution of 1:200

Applications for MMADHC Antibody - BSA Free

Application
Recommended Usage

Immunohistochemistry

1:20-1:200

Western Blot

1:500-1:2000

Formulation, Preparation, and Storage

Purification

Immunogen affinity purified

Formulation

PBS, 50% Glycerol, pH (7.3)

Format

BSA Free

Preservative

0.02% Sodium Azide

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 -20C. Avoid freeze-thaw cycles.

Background: MMADHC

MMADHC encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.

Alternate Names

cblD, chromosome 2 open reading frame 25, methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria, mitochondrial, protein C2orf25, mitochondrial

Gene Symbol

MMADHC

Additional MMADHC Products

Product Documents for MMADHC Antibody - BSA Free

Certificate of Analysis

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Product Specific Notices for MMADHC Antibody - BSA Free

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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Protocols

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FAQs

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