FAM161A Proteine
(Family with Sequence Similarity 161, Member A (FAM161A))
This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011].
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FAM161A
Spezies: Human
Wirt: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, SDS, WB
FAM161A
Spezies: Human
Wirt: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
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Aliase für FAM161A Proteine
family with sequence similarity 161 member A (FAM161A) Proteinefamily with sequence similarity 161, member A (Fam161a) Proteine
family with sequence similarity 161, member A (FAM161A) Proteine
4930430E16Rik Proteine
RGD1304999 Proteine
RP28 Proteine
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