S13A5 rabbit pAb
This gene encodes a protein belonging to the solute carrier family 13 group of proteins. This family member is a sodium-dependent citrate cotransporter that may regulate metabolic processes. Mutations in this gene cause early infantile epileptic encephalopathy 25. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014],
Product Specifications
Background
Product Name Alternative
Solute carrier family 13 member 5 (Na (+) /citrate cotransporter) (NaCT) (Sodium-coupled citrate transporter) (Sodium-dependent citrate transporter)
UniProt
Q86YT5
Swiss Prot
Q86YT5
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human S13A5 AA range: 313-363
Target
S13A5
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1:500-2000
Buffer
-20°C/1 year
Molecular Weight
60kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
60kD
Fragment
IgG
Subcellular Location
Cell membrane ; Multi-pass membrane protein .
Other Product Names
Solute carrier family 13 member 5 (Na (+) /citrate cotransporter) (NaCT) (Sodium-coupled citrate transporter) (Sodium-dependent citrate transporter)
Gene ID (Human)
284111
Available Sizes
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