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AHI1 Rabbit anti-Human, Mouse, Polyclonal, Proteintech
Rabbit Polyclonal Antibody
Marque: Proteintech 22045-1-AP-150UL
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Description
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.Spécification
AHI1 | |
Polyclonal | |
Unconjugated | |
AHI1 | |
AHI 1, AHI1, JBTS3, Jouberin, ORF1 | |
Rabbit | |
Antigen Affinity Chromatography | |
RUO | |
52906, 54806 | |
-20°C | |
Liquid |
Western Blot | |
0.18 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
Q8K3E5, Q8N157 | |
Ahi1 | |
AHI1 Fusion Protein Ag16885 | |
150 μL | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
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