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COPT1 rabbit pAb

CAT: 0855-ES11983-02Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0855-ES11983-02Size:100 µL
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Background
The protein encoded by this gene is a high-affinity copper transporter found in the cell membrane. The encoded protein functions as a homotrimer to effect the uptake of dietary copper. [provided by RefSeq, Aug 2011]
Description
The protein encoded by this gene is a high-affinity copper transporter found in the cell membrane. The encoded protein functions as a homotrimer to effect the uptake of dietary copper. [provided by RefSeq, Aug 2011],
UniProt
O15431
Swiss Prot
O15431
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from part region of human protein
Target
COPT1
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Buffer
-20°C/1 year
Molecular Weight
20kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
20kD
Fragment
IgG
Subcellular Location
Cell membrane; Multi-pass membrane protein. Localizes to the apical membrane in intestinal epithelial cells. .
Gene ID (Human)
1317

UniProtKB · O15431

High affinity copper uptake protein 1

COPT1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O15431
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
SLC31A1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A8K8Z6, Q53GR5, Q5T1M4
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Cellular component

Cell membraneEndosomeMembrane

Ligand

Copper

Biological process

Copper transportIon transportTransport

PTM

Disulfide bondGlycoproteinOxidationPhosphoprotein

Disease

EpilepsyNeurodegeneration

Domain

TransmembraneTransmembrane helix

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