RAB3GAP1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2730350

Détail du produit

Antigène: RAB3GAP1 (RAB3 GTPase Activating Protein Subunit 1 (Catalytic) (RAB3GAP1))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette RAB3GAP1 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human RAB3GAP1 / RAB3GAP (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: RAB3GAP1 (RAB3 GTPase Activating Protein Subunit 1 (Catalytic) (RAB3GAP1))

Autre désignation: Rab3gap1,rab3gap (RAB3GAP1 Produits)

Synonymes: 1700003B17Rik Protein, 4732493F09Rik Protein, AL117896 Protein, Rab3gap Protein, p130 Protein, P130 Protein, RAB3GAP Protein, RAB3GAP130 Protein, WARBM1 Protein, RAB3 GTPase activating protein subunit 1 Protein, RAB3 GTPase activating protein catalytic subunit 1 Protein, Rab3gap1 Protein, RAB3GAP1 Protein

Sujet: This gene encodes the catalytic subunit of a Rab GTPase activating protein. The encoded protein forms a heterodimer with a non-catalytic subunit to specifically regulate the activity of members of the Rab3 subfamily of small G proteins. This protein mediates the hydrolysis of GTP bound Rab3 to the GDP bound form. Mutations in this gene are associated with Warburg micro syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010].

Poids moléculaire: 111.7

NCBI Accession: NP_001165906