ASL Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2714867

Détail du produit

Antigène: ASL (Argininosuccinate Lyase (ASL))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

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

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

Attributs du produit:

• Recombinant human Arginosuccinase (transcript variant 1) 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: ASL (Argininosuccinate Lyase (ASL))

Autre désignation: Arginosuccinase (ASL Produits)

Synonymes: ASAL Protein, 2510006M18Rik Protein, zgc:63532 Protein, BA4879 Protein, PSPTO0125 Protein, Adl Protein, Asl Protein, argininosuccinate lyase Protein, argininosuccinate lyase ArgH Protein, adenylosuccinate lyase Protein, argininosuccinate lyase L homeolog Protein, ASL Protein, Asl Protein, asl Protein, argH2 Protein, argH Protein, arg7 Protein, CNC04420 Protein, STHERM_c13370 Protein, Adsl Protein, asl.L Protein, ARG7 Protein

Sujet: This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.

Poids moléculaire: 51.5 kDa

NCBI Accession: NP_001020114

Pathways: Response to Growth Hormone Stimulus