Search Thermo Fisher Scientific
- Contact Us
- Quick Order
-
Don't have an account ? Create Account
Search Thermo Fisher Scientific
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.
1700015F03Rik; Abelson helper integration site 1; abelson helper integration site 1 protein; abelson helper integration site 1 protein homolog; Ahi1; AHI-1; contatins SH3 and WD40 domains; D10Bwg0629e; dJ71N10.1; JBTS3; jouberin; ORF1; RP1-32B1.2
100 µL
100 µL
100 µL
100 µL
100 µL
100 µL
50 µg
100 µg
10 µL
Searching for an antibody we don't offer? We make custom antibodies for specific targets, species and applications.
More than 18,000 custom antibodies created so far.
Talk to a specialist nowIf an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support