AMPD1 Antibody

Novus Biologicals, part of Bio-Techne | Catalog # NBP1-81270

Novus Biologicals, part of Bio-Techne
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NBP1-81270
NBP1-81270-25ul
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Key Product Details

Species Reactivity

Validated:

Human

Predicted:

Mouse (92%), Rat (92%). Backed by our 100% Guarantee.

Applications

Immunohistochemistry, Immunohistochemistry-Paraffin

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Concentration

Concentrations vary lot to lot. See vial label for concentration. If unlisted please contact technical services.

View all AMPD1 Antibodies »

Product Specifications

Immunogen

This antibody was developed against Recombinant Protein corresponding to amino acids: SETSSTKLSHIDEYISSSPTYQTVPDFQRVQITGDYASGVTVEDFEIVCKGLYRALCIREKYMQKSFQRFPKTPSKYLRNIDGEAWVANE

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for AMPD1 Antibody

Immunohistochemistry-Paraffin: AMPD1 Antibody [NBP1-81270]

Immunohistochemistry-Paraffin: AMPD1 Antibody [NBP1-81270]

Immunohistochemistry-Paraffin: AMPD1 Antibody [NBP1-81270] - Staining of human skeletal muscle shows strong cytoplasmic positivity.

Applications for AMPD1 Antibody

Application
Recommended Usage

Immunohistochemistry

1:50 - 1:200

Immunohistochemistry-Paraffin

1:50 - 1:200
Application Notes
For IHC-Paraffin, HIER pH 6 retrieval is recommended.

Formulation, Preparation, and Storage

Purification

Immunogen affinity purified

Formulation

PBS (pH 7.2) and 40% Glycerol

Preservative

0.02% Sodium Azide

Concentration

Concentrations vary lot to lot. See 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: AMPD1

Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human.

Alternate Names

adenosine monophosphate deaminase 1, adenosine monophosphate deaminase 1 (isoform M), adenosine monophosphate deaminase-1 (muscle), AMP deaminase 1, AMP deaminase isoform M, AMPD, EC 3.5.4.6, MAD, MADA, Myoadenylate deaminase, skeletal muscle AMPD

Gene Symbol

AMPD1

Additional AMPD1 Products

Product Documents for AMPD1 Antibody

Product Datasheets

Certificate of Analysis

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

Download SDS

Product Specific Notices for AMPD1 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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