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Jouberin Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Marca: Invitrogen PA521895
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Descripción
Recommended positive controls: NT2D1. Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
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.
Especificaciones
| Jouberin | |
| Polyclonal | |
| Unconjugated | |
| AHI1 | |
| 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 | |
| Rabbit | |
| Antigen affinity chromatography | |
| RUO | |
| 54806 | |
| Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
| Liquid |
| Western Blot | |
| 1 mg/mL | |
| 0.1M tris glycine with 10% glycerol and 0.01% thimerosal; pH 7 | |
| Q8N157 | |
| AHI1 | |
| Synthetic peptide corresponding to a region within amino acids 1 and 42 of AHI1 (Uniprot ID#Q8N157) | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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