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Invitrogen™ CTR1 Recombinant Rabbit Monoclonal Antibody (23GB4635)

Description
CTR1 Recombinant Monoclonal Antibody for Flow, ICC/IF, Western Blot
The trace metal copper (Cu) plays a crucial role in mammalian cells as a cofactor for many enzymes. Cu-related genetic diseases, such as Menkes disease and Wilson disease, arise from a lack of Cu homeostasis in mammalian cells. CTR1 is a high-affinity copper-uptake protein. The C-terminal domain is similar to the Raf family of protein kinases, but it's first two-thirds encodes a novel protein domain. CTR1 provides the primary avenue for copper uptake in mammalian cells, thereby, affecting Cu homeostasis and embryonic development.
Specifications
Specifications
| Antigen | CTR1 |
| Applications | Flow Cytometry, Western Blot, Immunocytochemistry |
| Classification | Recombinant Monoclonal |
| Clone | 23GB4635 |
| Concentration | 0.25 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 |
| Gene | SLC31A1 |
| Gene Accession No. | O15431, Q8K211, Q9JK41 |
| Gene Alias | 4930445G01Rik; AI787263; AU016967; copper transport 1 homolog; copper transporter 1; Copper uptake transporter 1; COPT1; ctr1; ctr-1; hCTR1; high affinity copper uptake protein; high affinity copper uptake protein 1; high-affinity copper uptake protein; liver regeneration-related protein LRRGT00200; LRRGT00200; rCTR1; SLC31A1; slc31a1.L; solute carrier family 13 (sodium/sulphate symporters), member 1; solute carrier family 31 (copper transporter), member 1; solute carrier family 31 (copper transporter), member 1 L homeolog; solute carrier family 31 (copper transporters), member 1; solute carrier family 31 member 1; solute carrier family 31, member 1; Xctr1; XELAEV_18038194mg; zgc:76839 |
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