購物車
幫助
021-54845833/15800441009
中文名稱：兔抗AHI1多克隆抗體
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Background: |
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. |
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Applications: |
ELISA, IHC |
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Name of antibody: |
AHI1 |
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Immunogen: |
Synthetic peptide of humanAHI1 |
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Full name: |
Abelson helper integration site 1 |
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Synonyms： |
ORF1; AHI-1; JBTS3; dJ71N10.1 |
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SwissProt: |
Q8N157 |
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ELISA Recommended dilution: |
2000-5000 |
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IHC positive control: |
Human liver cancer |
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IHC Recommend dilution: |
25-100 |
