SLC25A16 Monoklonaler Antikörper

SLC25A16 Monoklonal Antikörper für WB, ELISA

Wirt / Isotyp

Maus / IgG1

Getestete Reaktivität

human

Anwendung

WB, ELISA

Konjugation

Unkonjugiert

CloneNo.

3F10C8

Kat-Nr. : 68107-1-Ig

Synonyme

hGP, Graves' didease protein, GDC, D10S105E, 3F10C8

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  WB analysis using 68107-1-Ig

  Various lysates were subjected to SDS PAGE followed by western blot with 68107-1-Ig (GDA antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. The membrane was stripped and reblotted with HRP-conjugated Beta Actin Monoclonal antibody (HRP-66009) as loading control.

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Geprüfte Anwendungen

• Erfolgreiche Detektion in WB: LNCaP-Zellen, HEK-293-Zellen, HeLa-Zellen, HepG2-Zellen, Jurkat-Zellen

Empfohlene Verdünnung

• Western Blot (WB): WB : 1:5000-1:50000

It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Sample-dependent, check data in validation data gallery

Produktinformation

68107-1-Ig bindet in WB, ELISA SLC25A16 und zeigt Reaktivität mit human

• Getestete Reaktivität: human
• Wirt / Isotyp: Maus / IgG1
• Klonalität: Monoklonal
• Typ: Antikörper
• Immunogen: SLC25A16 fusion protein Ag4891
• Vollständiger Name: solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16
• Berechnetes Molekulargewicht: 36 kDa
• Beobachtetes Molekulargewicht: 33 kDa
• GenBank-Zugangsnummer: BC030266
• Gene symbol: GDA
• Gene ID (NCBI): 8034
• Konjugation: Unkonjugiert
• Form: Liquid
• Reinigungsmethode: Protein-G-Reinigung
• Lagerungspuffer: PBS with 0.02% sodium azide and 50% glycerol
• Lagerungsbedingungen: Bei -20°C lagern. Nach dem Versand ein Jahr lang stabil Aliquotieren ist bei -20^oC Lagerung nicht notwendig. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

GDA, also named as SLC25A16, GDC, ML7, hML7, belongs to the mitochondrial carrier family. GDA encodes a protein that contains three tandemly repeated mitochondrial carrier protein domains. The encoded protein is localized in the mitochondrion inner membrane and facilitates the rapid transport and exchange of molecules between the cytosol and the mitochondrial matrix space. This gene has been associated with Graves' disease (PMID:11158296, 1457817).