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CLCN3 Rabbit Polyclonal Antibody (APC)

CAT: 0013-GTR18531895Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18531895Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Anti-CLCN3 Antibody. Tested in WB, Flow Cytometry, ELISA applications. This antibody reacts with Human.
Product Name Alternative
CLCN3; H (+/Cl (- exchange transporter 3; Chloride channel protein 3; ClC-3; Chloride transporter ClC-3
UniProt
P51790
Reactivity
Human, Rat
Immunogen
E.coli-derived human CLCN3 recombinant protein (Position: G293-R752) . Human CLCN3 shares 99.6% amino acid (aa) sequence identity with mouse CLCN3.
Target
H
Clonality
Polyclonal
Conjugation
APC
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Storage Conditions
At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
Notes
For research use only.
Applications Notes
Recommended applications are based on the parent unconjugated antibody. Customers may select suitable applications according to their experimental needs.
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Isotype
IgG

UniProtKB · P51790

H(+)/Cl(-) exchange transporter 3

CLCN3_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P51790
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CLCN3
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
B7Z932, B9EGJ9, D3DP34, E9PB97, O14918, Q86Z21
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Biological process

AntiportIon transportTransport

Ligand

ATP-bindingChlorideNucleotide-binding

Domain

CBS domainRepeatTransmembraneTransmembrane helix

Cellular component

Cell membraneCell projectionEndosomeGolgi apparatusLysosomeMembrane

Disease

Disease variantEpilepsyIntellectual disability

PTM

Glycoprotein

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