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Invitrogen™ SLC17A5 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA590456
Description
Immunogen sequence: MRSPVRDLAR NDGEESTDRT PLLPGAPRAE AAPVCCSARY NLAILAFFGF FIVYALRVNL SVALVDMVDS NTTLEDNRTS KACPEHSAPI KVHHNQTGKK; Positive Samples: 293T, SW480; Cellular Location: Cell membrane, Cytoplasmic vesicle, Lysosome membrane, Multi-pass membrane protein, secretory vesicle, synaptic vesicle membrane.
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; FLJ22227; FLJ23268; H(+)/nitrate cotransporter; H(+)/sialic acid cotransporter; hp59; 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 | |
Affinity chromatography | |
RUO | |
26503, 363103 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
ELISA, Western Blot | |
1.73 mg/mL | |
PBS with 50% glycerol and 0.01% thimerosal; pH 7.3 | |
Q9NRA2 | |
SLC17A5 | |
A synthetic peptide corresponding to a sequence within amino acids 1-100 of human SLC17A5 (NP_0365661). | |
100 μL | |
Primary | |
Human, Rat | |
Antibody | |
IgG |
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