Myosin VI Protein (MYO6) (Myc-DYKDDDDK Tag)

N° du produit ABIN2726687

Détail du produit

Antigène: Myosin VI (MYO6)

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

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

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

Attributs du produit:

• Recombinant human MYO6 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: Myosin VI (MYO6)

Autre désignation: Myo6 (MYO6 Produits)

Synonymes: 95F Protein, 95F MHC Protein, CG5695 Protein, Dm 95F Protein, Dm95F Protein, Dmel\\CG5695 Protein, Dro95F Protein, JAG Protein, Jaguar Protein, Jar Protein, M6 Protein, MHC95F Protein, MYOVI Protein, Mhc95F Protein, MyoVI Protein, Myosin VI Protein, jag Protein, ms(3)06746 Protein, myosins VI Protein, DFNA22 Protein, DFNB37 Protein, BC029719 Protein, Tlc Protein, sv Protein, RGD1560646 Protein, CMY6 Protein, jaguar Protein, myosin VI Protein, jar Protein, LOC373230 Protein, MYO6 Protein, myo6 Protein, Myo6 Protein

Sujet: This gene encodes a reverse-direction motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Poids moléculaire: 148.5 kDa

NCBI Accession: NP_004990

Pathways: Sensory Perception of Sound, Dicarboxylic Acid Transport, Asymmetric Protein Localization