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SLC17A5 Rabbit anti-Human, Polyclonal, Bioss

Rabbit Polyclonal Antibody
Supplier: Bioss BS24067R

Description
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.Specifications
SLC17A5 | |
Polyclonal | |
Unconjugated | |
SLC17A5 | |
4631416G20Rik; 4732491M05; AST; BOS_9478; FLJ22227; FLJ23268; H(+)/nitrate cotransporter; H(+)/sialic acid cotransporter; ISSD; Membrane glycoprotein HP59; Membrane glycoprotein SP55; NSD; proton-coupled sialic acid transporter; sb:cb809; SD; sialic acid storage disease; Sialin; SIASD; SLC17A5; SLD; Sodium/sialic acid cotransporter; solute carrier family 17 (acidic sugar transporter), member 5; solute carrier family 17 (anion/sugar transporter), member 5; Solute carrier family 17 member 5; SP55; Vesicular H(+)/Aspartate-glutamate cotransporter; zgc:153077 | |
Rabbit | |
Protein A | |
RUO | |
26503 | |
-20°C | |
Liquid |
ELISA, Western Blot | |
1 μg/mL | |
TBS with 1% BSA, 50% glycerol and 0.03% Proclin 300; pH | |
Q9NRA2 | |
SLC17A5 | |
KLH conjugated synthetic peptide derived from mouse SLC17A5. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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