BTR1 rabbit pAb
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BTR1 rabbit pAb
Background :
This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]Description :
This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010],Product Name Alternative :
SLC4A11; BTR1; Sodium bicarbonate transporter-like protein 11; Bicarbonate transporter-related protein 1; Sodium borate cotransporter 1; NaBC1; Solute carrier family 4 member 11UniProt :
Q8NBS3Swiss Prot :
Q8NBS3Reactivity :
Human; Rat; MouseImmunogen :
The antiserum was produced against synthesized peptide derived from human SLC4A11. AA range:291-340Target :
BTR1Clonality :
PolyclonalSource :
RabbitApplications :
WB; ELISAConcentration :
1 mg/mlDilution :
Western Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.Buffer :
-20°C/1 yearMolecular Weight :
100kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
100kDFragment :
IgGSubcellular Location :
Cell membrane ; Multi-pass membrane protein . Basolateral cell membrane ; Multi-pass membrane protein .Other Product Names :
SLC4A11; BTR1; Sodium bicarbonate transporter-like protein 11; Bicarbonate transporter-related protein 1; Sodium borate cotransporter 1; NaBC1; Solute carrier family 4 member 11Gene ID (Human) :
83959

