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Anticorps Polyclonal de lapin anti-SLC17A5

SLC17A5 Polyclonal Antibody for WB, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, rat, souris

Applications

WB, Indirect ELISA

Conjugaison

Non conjugué

N° de cat : 13320-1-PBS

Synonymes

Galerie de données de validation

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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.

Informations sur le produit

13320-1-PBS cible SLC17A5 dans les applications de WB, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat, souris

Réactivité Humain, rat, souris
Hôte / Isotype Lapin / IgG
Clonalité Polyclonal
Type Anticorps
Immunogène SLC17A5 Protéine recombinante Ag3855
Nom complet solute carrier family 17 (anion/sugar transporter), member 5
Masse moléculaire calculée 495 aa, 55 kDa
Poids moléculaire observé 31 kDa
Numéro d’acquisition GenBankBC020961
Symbole du gène SLC17A5
Identification du gène (NCBI) 26503
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par affinité contre l'antigène
Tampon de stockage PBS only
Conditions de stockageStore at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

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).

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