AMPD1 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2714666

Détail du produit

Antigène: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette AMPD1 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human AMP deaminase 1 / AMPD1 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: 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.

Détail du antigène

Antigène: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Autre désignation: Amp Deaminase 1,ampd1 (AMPD1 Produits)

Synonymes: 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

Sujet: 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].

Poids moléculaire: 90 kDa

NCBI Accession: NP_000027