Gephyrin Protein (GPHN) (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2721820

Détail du produit

Antigène: Gephyrin (GPHN)

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

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

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

Attributs du produit:

• Recombinant human Gephyrin (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: Gephyrin (GPHN)

Autre désignation: Gephyrin (GPHN Produits)

Synonymes: 5730552E08Rik Protein, AI662856 Protein, BC027112 Protein, C230040D23 Protein, GPH Protein, GPHRYN Protein, geph Protein, Geph Protein, GPHN Protein, GEPH Protein, HKPX1 Protein, gpgb1 Protein, DKFZp459M0825 Protein, gephyrin Protein, gephyrin L homeolog Protein, gephyrin a Protein, Gphn Protein, GPHN Protein, gphn.L Protein, gphna Protein, PTRG_08978 Protein, VDBG_00775 Protein, Tsp_03043 Protein, gphn Protein

Sujet: This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency. Numerous alternatively spliced transcript variants encoding different isoforms have been described however, the full-length nature of all transcript variants is not currently known.

Poids moléculaire: 83.3 kDa

NCBI Accession: NP_065857

Pathways: Synaptic Membrane, Skeletal Muscle Fiber Development