GFER-eiwit, menselijk, recombinant (HEK293, zijn)
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
Alterations in GFER gene have been associated with progressive mitochondrial myopathy, congenital cataracts, hearing loss, developmental delay, lactic acidosis and respiratory chain deficiency in 3 siblings born to consanguineous Moroccan parents by homozygosity mapping and candidate gene approach. Using homozygosity mapping, we discovered that a mutation in the GFER gene causes an infantile mitochondrial disorder.
Ice Packs
-20°C
Beschrijving
GFER-eiwit, menselijk, recombinant (HEK293, zijn) Beschikbaar in 5 µg. Bestel eenvoudig online met snelle levering.
Specificaties
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