AMPD1 Antibody - BSA Free

Novus Biologicals, part of Bio-Techne | Catalog # NBP3-03984

Novus Biologicals, part of Bio-Techne
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NBP3-03984-100ul
NBP3-03984-20ul
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Key Product Details

Species Reactivity

Validated:

Human, Mouse, Rat

Applications

Western Blot

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Format

BSA Free

Concentration

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

View all AMPD1 Antibodies »

Product Summary for AMPD1 Antibody - BSA Free

Immunogen

A synthetic peptide corresponding to a sequence within amino acids 1-100 of human AMPD1 (P23109). MNVRIFYSVSQSPHSLLSLLFYCAILESRISATMPLFKLPAEEKQIDDAMRNFAEKVFASEVKDEGGRQEISPFDVDEICPISHHEMQAHIFHLETLSTS

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for AMPD1 Antibody - BSA Free

Western Blot: AMPD1 AntibodyBSA Free [NBP3-03984]

Western Blot: AMPD1 AntibodyBSA Free [NBP3-03984]

Western Blot: AMPD1 Antibody [NBP3-03984] - Analysis of extracts of various cell lines, using AMPD1 antibody at 1:500 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit

Applications for AMPD1 Antibody - BSA Free

Application
Recommended Usage

Western Blot

1:500 - 1:2000
Please Note: Optimal dilutions of this antibody should be experimentally determined.

Formulation, Preparation, and Storage

Purification

Affinity purified

Formulation

PBS with 50% glycerol, pH7.3.

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: 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 - BSA Free

Product Datasheets

Certificate of Analysis

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Product Specific Notices for AMPD1 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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