ATL1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2715027

Détail du produit

Antigène: ATL1 (Atlastin GTPase 1 (ATL1))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette ATL1 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human Atlastin-1 / SPG3A (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: ATL1 (Atlastin GTPase 1 (ATL1))

Autre désignation: Atlastin-1,spg3a (ATL1 Produits)

Synonymes: ATL1 Protein, SPG3A Protein, fj46c01 Protein, wu:fj46c01 Protein, spg3a Protein, MGC146251 Protein, AD-FSP Protein, FSP1 Protein, GBP3 Protein, HSN1D Protein, SPG3 Protein, atlastin1 Protein, 4930435M24Rik Protein, Adfsp Protein, Fsp1 Protein, Spg3 Protein, Spg3a Protein, atlastin Protein, Atlastin-1 Protein, atlastin GTPase 1 Protein, ATL1 Protein, atl1 Protein, Atl1 Protein

Sujet: The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene.

Poids moléculaire: 63.4 kDa

NCBI Accession: NP_056999