AHI1 蛋白
(Abelson Helper Integration Site 1 (AHI1))
This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008].
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custom-made
AHI1
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
AHI1
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
Aliases for AHI1 蛋白
Abelson helper integration site 1 (AHI1) 蛋白Abelson helper integration site 1 (ahi1) 蛋白
Abelson helper integration site 1 (Ahi1) 蛋白
1700015F03Rik 蛋白
AHI-1 蛋白
Ahi-1 蛋白
AHI1 蛋白
D10Bwg0629e 蛋白
dJ71N10.1 蛋白
JBTS3 蛋白
ORF1 蛋白
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