AMPD1 Protein (Myc-DYKDDDDK Tag)

Produktnummer ABIN2714666

Produktdetails

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

Protein-Typ: Recombinant

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses AMPD1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

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

Produktmerkmale:

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

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

Anwendungsinformationen

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

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

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

Lagerung: -80 °C

Informationen zur Lagerung: 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.

Antigendetails

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

Andere Bezeichnung: Amp Deaminase 1,ampd1 (AMPD1 Produkte)

Synonyme: 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

Hintergrund: 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].

Molekulargewicht: 90 kDa

NCBI Accession: NP_000027