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SLC17A5 Polyklonaler Antikörper

SLC17A5 Polyklonal Antikörper für WB, Indirect ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, Indirect ELISA

Konjugation

Unkonjugiert

Kat-Nr. : 13320-1-PBS

Synonyme

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  • Western Blot (WB) analysis of human kidney tissue using SLC17A5 Polyclonal antibody (13320-1-AP)

    WB analysis of human kidney using 13320-1-AP (same clone as 13320-1-PBS)

    human kidney tissue were subjected to SDS PAGE followed by western blot with 13320-1-AP (SLC17A5 antibody) at dilution of 1:300 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 13320-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of HEK-293 cells using SLC17A5 Polyclonal antibody (13320-1-AP)

    WB analysis of HEK-293 using 13320-1-AP (same clone as 13320-1-PBS)

    HEK-293 cells were subjected to SDS PAGE followed by western blot with 13320-1-AP (SLC17A5 antibody) at dilution of 1:300 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 13320-1-PBS in a different storage buffer formulation.

Geprüfte Anwendungen

Produktinformation

13320-1-PBS bindet in WB, Indirect ELISA SLC17A5 und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
Wirt / Isotyp Kaninchen / IgG
Klonalität Polyklonal
Typ Antikörper
Immunogen SLC17A5 fusion protein Ag3855
Vollständiger Name solute carrier family 17 (anion/sugar transporter), member 5
Berechnetes Molekulargewicht 495 aa, 55 kDa
Beobachtetes Molekulargewicht 31 kDa
GenBank-ZugangsnummerBC020961
Gene symbol SLC17A5
Gene ID (NCBI) 26503
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Antigen-Affinitätsreinigung
Lagerungspuffer PBS only
LagerungsbedingungenStore at -80°C. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

SLC17A5 encodes a transmembrane protein, sialin, which transports free sialic acid across the lysosomal membrane. Mutations in sialin result in neurodegenerative sialic acid storage disorders, Salla disease (SD) and infantile sialic acid storage disease (ISSD). In the central nervous system, sialin is more abundant in neurons than in glia. It has been reported to be localized into lysosome in neuron but in plasma membrane in nonneuronal cells (PMID: 15006695).