AHI1 ELISA试剂盒
(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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6 results
AHI1
适用: 大鼠
Colorimetric
Sandwich ELISA
0.156 ng/mL - 10 ng/mL
Cell Lysate, Tissue Homogenate
AHI1
适用: 人
Colorimetric
Sandwich ELISA
0.313 ng/mL - 20 ng/mL
Cell Lysate, Tissue Homogenate
AHI1
适用: 小鼠
Colorimetric
Sandwich ELISA
78 pg/mL - 5000 pg/mL
Cell Lysate, Tissue Homogenate
Aliases for AHI1 ELISA试剂盒
Abelson helper integration site 1 (AHI1) ELISA试剂盒Abelson helper integration site 1 (ahi1) ELISA试剂盒
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