Syntaxin 1B Protein (STX1B) (Myc-DYKDDDDK Tag)

N° du produit ABIN2733109

Détail du produit

Antigène: Syntaxin 1B (STX1B)

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette Syntaxin 1B protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human Syntaxin 1B / STX1B 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: Syntaxin 1B (STX1B)

Autre désignation: Syntaxin 1b,stx1b (STX1B Produits)

Synonymes: STX1B2 Protein, STX1B Protein, stx1b1 Protein, stx1b2 Protein, STX1B1 Protein, Stx1b2 Protein, Stx1bl Protein, Syn1b Protein, Stx2 Protein, syntaxin1b Protein, wu:fb76h10 Protein, zgc:92909 Protein, syntaxin 1B Protein, syntaxin 1A Protein, syntaxin 1B L homeolog Protein, syntaxin1B Protein, STX1B Protein, STX1A Protein, stx1b Protein, LOC100136181 Protein, stx1b.L Protein, Stx1b Protein

Sujet: The protein encoded by this gene belongs to a family of proteins thought to play a role in the exocytosis of synaptic vesicles. Vesicle exocytosis releases vesicular contents and is important to various cellular functions. For instance, the secretion of transmitters from neurons plays an important role in synaptic transmission. After exocytosis, the membrane and proteins from the vesicle are retrieved from the plasma membrane through the process of endocytosis. Mutations in this gene have been identified as one cause of fever-associated epilepsy syndromes. A possible link between this gene and Parkinson's disease has also been suggested.

Poids moléculaire: 33.1 kDa

NCBI Accession: NP_443106