Tag | C-Flag Taq |
---|---|
Target | |
Synonyms | HKPX1, STHE |
Description | Human GLRA1 full length protein-synthetic nanodisc |
Delivery | 6~8weeks |
Uniprot ID | P23415 |
Expression Host | HEK293 |
Protein Families | Ion Channels: Cys-loop Receptors |
Protein Pathways | N/A |
Molecular Weight | The human full length GLRA1 protein has a MW of 52.6kDa |
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 specific instructions. Do not use solvents with pH lower than 6.5 in subsequent experiments. |
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 protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor, which mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Multiple transcript variants encoding different isoforms have been found. [provided by RefSeq, Dec 2015] |
Usage | Research use only |
Human GLRA1 full length protein-synthetic nanodisc
Price: 10 μg $900.00 ; 50 μg $4400.00 ; 100 μg $8000.00
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