Rabbit Polyclonal antibody to AHI1 (Abelson helper integration site 1)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]
Immunogen
Recombinant protein encompassing a sequence within the N-terminus region of human AHI1. The exact sequence is proprietary.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WB
*Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity
Human
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Gene Synonyms
AHI-1 antibody, DKFZp686J1653 antibody, FLJ14023 antibody, FLJ20069 antibody, JBTS3 antibody, ORF1 antibody, dJ71N10.1 antibody, AHI1 antibody, abelson helper integration site 1 protein homolog antibody, contatins SH3 and WD40 domains antibody, jouberin an
Molecular Weight(MW)
137 kDa (note) (5)
Application
Application
Sample (30 ug of whole cell lysate) A: NT2D1 7.5% SDS PAGE diluted at 1:1000
Application Notes
*Optimal dilutions/concentrations should be determined by the researcher.
Additional Information
Form
Liquid
Storage Instructions
Keep as concentrated solution. Aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Storage Buffer
0.1M Tris, 0.1M Glycine, 20% Glycerol (pH7). 0.01% Thimerosal was added as a preservative.