SLC17A5 Polyclonal Antibody, AbBy Fluor™ 488 Conjugated
Product Specifications
Background
This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]
Synonyms
AST; H (+) /nitrate cotransporter; H (+) /sialic acid cotransporter; ISSD; Membrane glycoprotein HP59; NSD; S17A5_MOUSE; SD; Sialic acid storage disease; Sialin; SIASD; Slc17a5; SLD; Solute carrier family 17 (anion/sugar transportermember 5; Solute carrier family 17 member 5; Vesicular H (+) /Aspartate-glutamate cotransporter.
Gene ID
235504
Swiss Prot
Q8BN82
Cellular Locus
Cell membrane
Host
Rabbit
Cross Reactivity
Mouse
Immunogen
201-300/495
Target
SLC17A5
Clonality
Polyclonal
Isotype
IgG
Conjugation
AbBy Fluor™ 488
Source
KLH conjugated synthetic peptide derived from mouse SLC17A5
Applications
WB
Purification
Purified by Protein A.
Excitation Emission
499nm/519nm
Concentration
1µg/µl
Dilution
WB (1:300-5000)
Buffer
Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Modification
Unmodified
Storage Conditions
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Gene ID URL
235504
Predicted Cross Reactivity
Rat, Cow, Sheep, Rabbit
Curated Selection
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