中文 
别名:TC1; THT1; TRMA; THMD1; THTR1应用:IHC
反应种属:Human
规格：50μl/100μl
| Description |
|---|
| This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. |
| Specification | |
|---|---|
| Aliases | TC1; THT1; TRMA; THMD1; THTR1 |
| Swissprot | O60779 |
| 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 SLC19A2 |
| Formulation | pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Application | |
|---|---|
| IHC | 1/15-1/50 |
| ELISA | 1/1000-1/2000 |
 |
The image is immunohistochemistry of paraffin-embedded Human brain tissue using P07601(SLC19A2 Antibody) at dilution 1/15. (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。
暂无评论
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。
发表回复