AMPD1 Antibody

Novus Biologicals, part of Bio-Techne | Catalog # NBP2-24509

Novus Biologicals, part of Bio-Techne

Key Product Details

Species Reactivity

Validated:

Human, Mouse, Rat, Bovine, Canine, Opossum, Primate

Cited:

Mouse

Applications

Validated:

Immunohistochemistry, Immunohistochemistry-Paraffin, Western Blot

Cited:

Western Blot

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Concentration

1.0 mg/ml

View all AMPD1 Antibodies »

Product Specifications

Immunogen

A portion of amino acids 140-190 of human AMPDA1 was used as the immunogen.

Reactivity Notes

100% homologous in human (isoforms CRA_a and CRA_c), mouse, rat (isoforms CRA_a and CRA_b).

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for AMPD1 Antibody

Western Blot: AMPD1 Antibody [NBP2-24509]

Western Blot: AMPD1 Antibody [NBP2-24509]

Western Blot: AMPD1 Antibody [NBP2-24509] - Analysis of human AMPDA1 in mouse skeletal muscle lysate in the 1) absence, 2) presence of immunizing peptide and 3) rat skeletal muscle using NBP2-24509 at 1 ug/ml.
Immunohistochemistry-Paraffin: AMPD1 Antibody [NBP2-24509]

Immunohistochemistry-Paraffin: AMPD1 Antibody [NBP2-24509]

Immunohistochemistry-Paraffin: AMPD1 Antibody [NBP2-24509] - Analysis of human skeletal muscle using NBP2-24509 at 10 ug/ml.

Applications for AMPD1 Antibody

Application
Recommended Usage

Immunohistochemistry-Paraffin

10 ug/ml

Western Blot

0.5-2 ug/ml

Formulation, Preparation, and Storage

Purification

Immunogen affinity purified

Formulation

PBS

Preservative

0.05% Sodium Azide

Concentration

1.0 mg/ml

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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