AMPD1 Antibody - BSA Free

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Western Blot: AMPD1 Antibody - BSA Free [NBP3-48169] - Mouse skeletal muscle tissue were subjected to SDS PAGE followed by western blot with (AMPD1 antibody) at dilution of 1:300

Product Details

Summary
Reactivity Hu, Mu, RtSpecies Glossary
Applications WB, ELISA
Clonality
Polyclonal
Host
Rabbit
Conjugate
Unconjugated
Format
BSA Free

Order Details

AMPD1 Antibody - BSA Free Summary

Description
Novus Biologicals Rabbit AMPD1 Antibody - BSA Free (NBP3-48169) is a polyclonal antibody validated for use in WB and ELISA. All Novus Biologicals antibodies are covered by our 100% guarantee.
Immunogen
adenosine monophosphate deaminase 1(isoform M). (Uniprot# P23109)
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
AMPD1
Purity
Immunogen affinity purified
Innovator's Reward
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Applications/Dilutions

Dilutions
  • ELISA
  • Western Blot 1:500-1:5000
Theoretical MW
80 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.

Packaging, Storage & Formulations

Storage
Store at -20C. Avoid freeze-thaw cycles.
Buffer
PBS, 50% Glycerol, pH (7.3)
Preservative
0.02% Sodium Azide
Purity
Immunogen affinity purified

Alternate Names for AMPD1 Antibody - BSA Free

  • adenosine monophosphate deaminase 1 (isoform M)
  • adenosine monophosphate deaminase 1
  • 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

Background

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.

Limitations

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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Product General Protocols

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol AMPD1