中文 
别名:ORF1; AHI-1; JBTS3; dJ71N10.1应用:IHC
反应种属:Human
规格：50μl/100μl
| 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. |
| Specification | |
|---|---|
| Aliases | ORF1; AHI-1; JBTS3; dJ71N10.1 |
| Entrez GeneID | 54806; |
| Swissprot | Q8N157 |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human |
| Immunogen | Synthetic peptide of human Abelson helper integration site 1 |
| Formulation | Rabbit IgG in pH7.4 PBS, 0.05% NaN3, 40% Glycerol. |
| Application | |
|---|---|
| IHC | 1/25-1/100 |
 |
Immunohistochemical analysis of paraffin-embedded Human liver cancer tissue using P42991 at dilution 1/25. |
本公司的所有产品仅用于科学研究或者工业应用等非医疗目的，不可用于人类或动物的临床诊断或治疗，非药用，非食用。
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本公司的所有产品仅用于科学研究或者工业应用等非医疗目的，不可用于人类或动物的临床诊断或治疗，非药用，非食用。
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