SLC39A5 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2735909

Détail du produit

Antigène: SLC39A5 (Solute Carrier Family 39 (Metal Ion Transporter), Member 5 (SLC39A5))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette SLC39A5 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human Zinc transporter ZIP5 / SLC39A5 (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: SLC39A5 (Solute Carrier Family 39 (Metal Ion Transporter), Member 5 (SLC39A5))

Autre désignation: Zinc Transporter Zip5,slc39a5 (SLC39A5 Produits)

Synonymes: 1810013D05Rik Protein, 2010205A06Rik Protein, Zip5 Protein, LZT-Hs7 Protein, ZIP5 Protein, solute carrier family 39 member 5 Protein, solute carrier family 39 (metal ion transporter), member 5 Protein, SLC39A5 Protein, Slc39a5 Protein

Sujet: The protein encoded by this gene belongs to the ZIP family of zinc transporters that transport zinc into cells from outside, and play a crucial role in controlling intracellular zinc levels. Zinc is an essential cofactor for many enzymes and proteins involved in gene transcription, growth, development and differentiation. Mutations in this gene have been associated with autosomal dominant high myopia (MYP24). Alternatively spliced transcript variants have been found for this gene.

Poids moléculaire: 56.1 kDa

NCBI Accession: NP_775867

Pathways: Transition Metal Ion Homeostasis