| Tag | C-Flag Tag |
|---|---|
| Target | |
| Synonyms | ACHRD, CMS2A, CMS3A, CMS3B, CMS3C, FCCMS, SCCMS |
| Description | Human ACHD full length protein-synthetic nanodisc |
| Delivery | 6~8weeks |
| Uniprot ID | Q07001 |
| Expression Host | HEK293 |
| Protein Families | Ion Channels: Cys-loop Receptors |
| Protein Pathways | N/A |
| Molecular Weight | The human full length ACHD protein has a MW of 58.9kDa |
| Formulation & Reconstitution | Lyophilized from nanodisc solubilization buffer (20 mM Tris-HCl, 150 mM NaCl, pH 8.0). Normally 5% – 8% trehalose is added as protectants before lyophilization. Please see Certificate of Analysis for |
| Storage & Shipping | Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature. |
| Background | The acetylcholine receptor of muscle has 5 subunits of 4 different types: 2 alpha and 1 each of beta, gamma and delta subunits. After acetylcholine binding, the receptor undergoes an extensive conformation change that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Defects in this gene are a cause of multiple pterygium syndrome lethal type (MUPSL), congenital myasthenic syndrome slow-channel type (SCCMS), and congenital myasthenic syndrome fast-channel type (FCCMS). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015] |
| Usage | Research use only |
| Conjugate | Unconjugated |
Human ACHD full length protein-synthetic nanodisc
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