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Sino Biological Inc. liefert Cynomolgus ALK-7 / ALK7 / ACVR1C Protein mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.
Weitere Informationen über Cynomolgus ALK-7 / ALK7 / ACVR1C Protein lesen Sie bitte: http://www.sinobiological.com/ALK-7-ALK7-ACVR1C-Protein-g-10179.html
| Synonym | ACVR1C |
| Protein Construction | A DNA sequence encoding the cynomolgus ACVR1C (F7GDQ6) (Leu44-Glu113) was expressed, fused with the Fc region of human IgG1 at the C-terminus. |
| Source | Cynomolgus |
| Expression Host | Human Cells |
| Purity | > 95 % as determined by SDS-PAGE | SDS-PAGE:![]() ALK-7 protein |
| Endotoxin | < 1.0 EU per μg of the protein as determined by the LAL method | |
| Stability | Samples are stable for up to twelve months from date of receipt at -70℃ | |
| Predicted N terminal | Gly 25 | |
| Molecular Mass | The recombinant cynomolgus ACVR1C is a disulfide-linked homodimer. The reduced monomer comprises 330 amino acids and has a calculated molecular mass of 36.6 KDa.The apparent molecular mass of cynomolgus CD38 is approximately 42-46 KDa respectively in SDS-PAGE. | |
| Formulation | Lyophilized from sterile PBS, pH7.4
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| Storage | Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles. |
| Reconstitution | A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information. |
ALK-7, also known as ALK7 and ACVR1C, is a member of the ALK family. ALK-7 is a serine-threonine kinase that can cause the activation of one of the SMAD signal transducers, SMAD2. It induces cell death by apoptosis through activation of the traditional TGF-beta pathway components in a process involving activation of SMAD2, SMAD3, caspase-3 and caspase-9. ALK-7 has a ligand known as Nodal. Nodal stimulates the secretion of TIMP-1 and inhibits matrix metalloproteinases MMP-2 and MMP-9 activity. The overexpression of Nodal or constitutively active ALK-7 decreases cell migration and invasion, whereas knock-down of Nodal and ALK-7 has the opposite effects.