ÖÐÎÄÃû³Æ£º Íÿ¹TSPEAR¶à¿Ë¡¿¹Ìå
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Background: |
This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. |
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Applications: |
ELISA, IHC |
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Name of antibody: |
TSPEAR |
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Immunogen: |
Fusion protein of human TSPEAR |
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Full name: |
thrombospondin-type laminin G domain and EAR repeats |
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Synonyms£º |
DFNB98; TSP-EAR; C21orf29 |
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SwissProt: |
Q8WU66 |
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ELISA Recommended dilution: |
1000-5000 |
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IHC positive control: |
Human thyroid cancer and Human liver cancer |
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IHC Recommend dilution: |
50-200 |
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021-54845833/15800441009
