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Slc25a46

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SLC25A46 is a gene that encodes a mitochondrial carrier protein. This protein is involved in the transport of various metabolites and ions across the mitochondrial membrane.

Automatically generated - may contain errors

Lab products found in correlation

Mitofilin myc, by OriGene (2 mentions) Pcdna3, by Thermo Fisher Scientific (2 mentions)

2 protocols using slc25a46

1

Generating Fluorescent Protein Constructs

Check if the same lab product or an alternative is used in the 5 most similar protocols
HB9:Gal4-VP16 was generated from the pmT hb9s YFP kindly provided by the Nonet Lab at Wash U. UAS-E1b:mYFP,mitoCFP was kindly provided by Bettina Schmid36 (link) from the German Center for Neurodegenerative Diseases (DZNE). SLC25A46 and mitofilin-myc were obtained from (Origene). SLC25A46 was subcloned into pcDNA3.1 (Invitrogen) with either C-terminal HA or myc. For RNA synthesis SLC25A46-HA was also subcloned into PCS2+.
Abrams A.J., Hufnagel R.B., Rebelo A., Zanna C., Patel N., Gonzalez M.A., Campeanu I.J., Griffin L.B., Groenewald S., Strickland A.V., Tao F., Speziani F., Abreu L., Schüle R., Caporali L., La Morgia C., Maresca A., Liguori R., Lodi R., Ahmed Z.M., Sund K.L., Wang X., Krueger L.A., Peng Y., Prada C.E., Prows C.A., Bove K., Schorry E.K., Antonellis A., Zimmerman H.H., Abdul-Rahman O.A., Yang Y., Downes S.M., Prince J., Fontanesi F., Barrientos A., Nemeth A.H., Carelli V., Huang T., Zuchner S, & Dallman J.E. (2015). Mutations in the UGO1-like protein SLC25A46 cause an optic atrophy spectrum disorder. Nature genetics, 47(8), 926-932.
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2

Generating Fluorescent Protein Constructs

Check if the same lab product or an alternative is used in the 5 most similar protocols
HB9:Gal4-VP16 was generated from the pmT hb9s YFP kindly provided by the Nonet Lab at Wash U. UAS-E1b:mYFP,mitoCFP was kindly provided by Bettina Schmid36 (link) from the German Center for Neurodegenerative Diseases (DZNE). SLC25A46 and mitofilin-myc were obtained from (Origene). SLC25A46 was subcloned into pcDNA3.1 (Invitrogen) with either C-terminal HA or myc. For RNA synthesis SLC25A46-HA was also subcloned into PCS2+.
Abrams A.J., Hufnagel R.B., Rebelo A., Zanna C., Patel N., Gonzalez M.A., Campeanu I.J., Griffin L.B., Groenewald S., Strickland A.V., Tao F., Speziani F., Abreu L., Schüle R., Caporali L., La Morgia C., Maresca A., Liguori R., Lodi R., Ahmed Z.M., Sund K.L., Wang X., Krueger L.A., Peng Y., Prada C.E., Prows C.A., Bove K., Schorry E.K., Antonellis A., Zimmerman H.H., Abdul-Rahman O.A., Yang Y., Downes S.M., Prince J., Fontanesi F., Barrientos A., Nemeth A.H., Carelli V., Huang T., Zuchner S, & Dallman J.E. (2015). Mutations in the UGO1-like protein SLC25A46 cause an optic atrophy spectrum disorder. Nature genetics, 47(8), 926-932.
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