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Western Blot (WB) (Western Blot analysis of AMPD1 in Human fetal muscle tissue using AMPD1 Rabbit pAb at dilution 1/1600)

Rabbit anti-Human AMPD1 Polyclonal Antibody | anti-AMPD1 antibody

AMPD1 Rabbit pAb

Gene Names
AMPD1; MAD; MADA
Reactivity
Human
Applications
Western Blot, Immunohistochemistry
Purity
Affinity purified
Synonyms
AMPD1; Polyclonal Antibody; AMPD1 Rabbit pAb; adenosine monophosphate deaminase 1; MAD; MADA; anti-AMPD1 antibody
Ordering
For Research Use Only!
Host
Rabbit
Reactivity
Human
Clonality
Polyclonal
Isotype
IgG
Purity/Purification
Affinity purified
Form/Format
pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Concentration
0.5mg/ml (varies by lot)
Applicable Applications for anti-AMPD1 antibody
Western Blot (WB), Immunohistochemistry-Paraffin (IHC-P)
Application Notes
WB: 1:500-1:2000
IHC-P: 1:100-1:300
Immunogen
Synthetic peptide of human AMPD1
Conjugation
Unconjugated
Modification
Unmodified
Preparation and Storage
Store at 4 degree C for short term. Store at -20 degree C for long term. Avoid freeze/thaw cycle.

Western Blot (WB)

(Western Blot analysis of AMPD1 in Human fetal muscle tissue using AMPD1 Rabbit pAb at dilution 1/1600)

Western Blot (WB) (Western Blot analysis of AMPD1 in Human fetal muscle tissue using AMPD1 Rabbit pAb at dilution 1/1600)

Immunohistochemistry (IHC)

(Immunohistochemistry of AMPD1 in paraffin-embedded Human liver cancer tissue using AMPD1 Rabbit pAb at dilution 1/70. Predicted cell location: Cytoplasm)

Immunohistochemistry (IHC) (Immunohistochemistry of AMPD1 in paraffin-embedded Human liver cancer tissue using AMPD1 Rabbit pAb at dilution 1/70. Predicted cell location: Cytoplasm)
Related Product Information for anti-AMPD1 antibody
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. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
270
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
90,219 Da
NCBI Official Full Name
AMP deaminase 1 isoform 1
NCBI Official Synonym Full Names
adenosine monophosphate deaminase 1
NCBI Official Symbol
AMPD1
NCBI Official Synonym Symbols
MAD; MADA
NCBI Protein Information
AMP deaminase 1; AMPD; skeletal muscle AMPD; myoadenylate deaminase; adenosine monophosphate deaminase-1 (muscle); adenosine monophosphate deaminase 1 (isoform M)
UniProt Protein Name
AMP deaminase 1
Protein Family
UniProt Gene Name
AMPD1
UniProt Entry Name
AMPD1_HUMAN

NCBI Description

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. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]

Uniprot Description

AMPD1: AMP deaminase plays a critical role in energy metabolism. Defects in AMPD1 are the cause of adenosine monophosphate deaminase deficiency muscle type (AMPDDM). AMPDDM is a metabolic disorder resulting in exercise-related myopathy. It is characterized by exercise-induced muscle aches, cramps, and early fatigue. Belongs to the adenosine and AMP deaminases family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Nucleotide Metabolism - purine; EC 3.5.4.6; Hydrolase

Chromosomal Location of Human Ortholog: 1p13

Cellular Component: cytosol

Molecular Function: metal ion binding; AMP deaminase activity; myosin heavy chain binding

Biological Process: response to organic substance; IMP salvage; nucleobase, nucleoside and nucleotide metabolic process; purine salvage; purine base metabolic process

Disease: Myopathy Due To Myoadenylate Deaminase Deficiency

Research Articles on AMPD1

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Product Notes

The AMPD1 ampd1 (Catalog #AAA4759572) is an Antibody produced from Rabbit and is intended for research purposes only. The product is available for immediate purchase. The AMPD1 Rabbit pAb reacts with Human and may cross-react with other species as described in the data sheet. AAA Biotech's AMPD1 can be used in a range of immunoassay formats including, but not limited to, Western Blot (WB), Immunohistochemistry-Paraffin (IHC-P). WB: 1:500-1:2000 IHC-P: 1:100-1:300. Researchers should empirically determine the suitability of the AMPD1 ampd1 for an application not listed in the data sheet. Researchers commonly develop new applications and it is an integral, important part of the investigative research process. It is sometimes possible for the material contained within the vial of "AMPD1, Polyclonal Antibody" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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