中文 
别名:DFNB98; TSP-EAR; C21orf29应用:IHC
反应种属:Human
规格：50μl/100μl
| Description |
|---|
| 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. |
| Specification | |
|---|---|
| Aliases | DFNB98; TSP-EAR; C21orf29 |
| Swissprot | Q8WU66 |
| Host/Isotype | Rabbit IgG |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human |
| Immunogen | Fusion protein of human TSPEAR |
| Formulation | pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Application | |
|---|---|
| IHC | 1/50-1/200 |
| ELISA | 1/1000-1/5000 |
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The image is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using P07997(TSPEAR Antibody) at dilution 1/50. (Original magnification: ×200) |
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The image is immunohistochemistry of paraffin-embedded Human liver cancer tissue using P07997(TSPEAR Antibody) at dilution 1/50. (Original magnification: ×200) |
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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