蛋白
抗体
检测试剂盒
蛋白MARKER
分子生物学
规格：
查看说明书TRPM7 Rabbit pAb
Cat#:DPA03766应用：WB,ICC/IF,FC
| Product Name: | TRPM7 Rabbit pAb |
| Cat No.: | DPA03766 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,ICC/IF,FC |
| Recommended Dilution: | WB: 1:1000-1:2000 ICC/IF: 1:20-1:100 FC: 1:50 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | A synthetic peptide of human TRPM7 |
| Calculated Molecular Weight: | 213 kDa |
| Observed Molecular Weight: | 213 kDa |
| GenBank Accession Number: | Q96QT4 |
| Gene ID (NCBI): | 54822 |
| Synonyms: | CHAK; CHAK1; ALSPDC; LTRPC7; LTrpC-7; TRP-PLIK |
| Background: | This gene belongs to the melastatin subfamily of transient receptor potential family of ion channels. The protein encoded by this gene is both an ion channel and a serine/threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. The encoded protein is involved in cytoskeletal organization, cell adhesion, cell migration and organogenesis. Defects in this gene are a cause of amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam. The gene may also be associated with defects of cardiac function. [provided by RefSeq, Aug 2017] |
| Category: | Primary Ab |
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