AMPD1 Protein (Myc-DYKDDDDK Tag)
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- Target See all AMPD1 Proteins
- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This AMPD1 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human AMP deaminase 1 / AMPD1 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product AMPD1 Protein
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
- Alternative Name
- Amp Deaminase 1,ampd1 (AMPD1 Products)
- Synonyms
- ampd1 Protein, MAD Protein, MADA Protein, AI553520 Protein, Ampd-1 Protein, Ampd01 Protein, RATAMPD01 Protein, zgc:77905 Protein, adenosine monophosphate deaminase 1 Protein, N-acetyl-anhydromuranmyl-L-alanine amidase Protein, N-acetylmuramoyl-L-alanine amidase Protein, Negative regulator of beta-lactamase expression Protein, adenosine monophosphate deaminase 1 (isoform M) Protein, AMPD1 Protein, ampD1 Protein, ampd1 Protein, Ampd1 Protein
- 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. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010].
- Molecular Weight
- 90 kDa
- NCBI Accession
- NP_000027
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