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Background: |
SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition. |
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Applications: |
ELISA, IHC |
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Name of antibody: |
SNX29 |
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Immunogen: |
Synthetic peptide of human SNX29 |
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Full name: |
sorting nexin 29 |
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Synonyms: |
RUNDC2A; A-388D4.1 |
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SwissProt: |
Q8TEQ0 |
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ELISA Recommended dilution: |
1000-2000 |
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IHC positive control: |
Human liver cancer and Human colon cancer |
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IHC Recommend dilution: |
25-100 |
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