human AHI1 shRNA silencing AAV

Cat. No: shAAV-200608

Availability: 4-5 weeks

Name: AAV-h-AHI1-shRNA

This is an AAV expressing shRNA for silencing of Human AHI1.

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Viral Backbone: Recombinant AAV
AAV-ITR: AAV2
AAV Serotype: Available in AAV1, AAV2, AAV3, AAV5, AAV6, AAV8, AAV9, AAV-DJ, AAV-DJ8, AAV-DJ9 and other wildtype/synthetic AAV capsids
Promoter: U6
Reporter: eGFP (default), optional CFP, YFP, RFP, mCherry
Storage Buffer: PBS/5% Glycerol

Species: Human
Gene Symbol: AHI1
Gene Name: Abelson helper integration site 1
Gene ID: 54806
Gene Synonyms: AHI-1; dJ71N10.1; JBTS3; ORF1
ORF Size: 1830 bp
RefSeq#: NM_017651
Gene Description: AHI1 is apparently required for both cerebellar and cortical development in humans. AHI1 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.
UniGene ID: Hs.386684
HGNC ID: HGNC:21575