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| Synonym | CANT1, SHAPY |
| Protein Construction | A DNA sequence encoding the human CANT1(Q8WVQ1-1)(Gly80-Ile401) was expressed ,with the fused Fc region of human IgG1 at the N-terminus. |
| Source | Human |
| Expression Host | Human Cells |
| Purity | > 90 % as determined by SDS-PAGE | SDS-PAGE:![]() CANT1 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 | Glu | |
| Molecular Mass | The recombinant human CANT1/Fc is a disulfide-linked homodimer. The reduced monomer comprises 582 amino acids and has a predicted molecular mass of 64.3 kDa. The apparent molecular mass of the protein is approximately 65 kDa in SDS-PAGE under reducing conditions due to glycosylation. | |
| Formulation | Lyophilized from a 0.2μm filtered solution of 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. |
| Molecule | Species | Description //For Detailed Info. and Price------CLICK! | Cat. No |
| CANT1 | Human | CANT1 Protein, Recombinant | 13124-H01H |
| CANT1 | Human | CANT1 Protein, Recombinant | 13124-H07H |
CANT1(calcium activated nucleotidase 1, N-Histidine-tagged) belongs to the apyrase family. It functions as a calcium-dependent nucleotidase with a preference for UDP. Alternatively spliced transcript variants have been noted for this gene. Defects in CANT1 are the cause of desbuquois dysplasia. A chondrodysplasia characterized by severe prenatal and postnatal growth retardation (less than -5 SD), joint laxity, short extremities, progressive scoliosis, round face, midface hypoplasia, prominent bulging eyes. The main radiologic features are short long bones with metaphyseal splay, a 'Swedish key' appearance of the proximal femur (exaggerated trochanter), and advance carpal and tarsal bone age. Two forms of desbuquois dysplasia are distinguished on the basis of the presence (type 1) or absence (type 2) of characteristic hand anomalies: an extra ossification center distal to the second metacarpal, delta phalanx, bifid distal thumb phalanx, and phalangeal dislocations.
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