SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
AHI1-C12orf50-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
AHI1-C12orf50-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
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]
Gene Symbol : AHI1
Gene Name : Abelson helper integration site 1
Chromosome : CHR 6: 135,497,774-135,283,971
Locus : 6q23.3
Gene Symbol : C12ORF50
Gene Name : Chromosome 12 open reading frame 50
Chromosome : CHR 12: 880,293,98-879,800,38
Locus : 12q21.32
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.