Nanodisc Human SLC25A4 Protein (HDFP015)
- SKU:
- HDFP015
- Product Type:
- Recombinant Protein
- Protein Type:
- Full-Length Bioactive Membrane Protein
- Species:
- Human
- Uniprot:
- P12235
Frequently bought together:
Description
system_update_altDatasheet
Product name | Human SLC25A4 full length protein-synthetic nanodisc |
Size: | 10ug |
Product SKU: | HDFP015 |
Product Category | Full Length Transmembrane Proteins |
Target: | SLC25A4 |
Uniprot: | P12235 |
Description: | Human SLC25A4 full length protein-synthetic nanodisc |
Molecular Weight: | The human full length SLC25A4 protein has a MW of 33.1 kDa |
Protein Family: | Druggable Genome, Transmembrane |
Protein Pathways: | Calcium signaling pathway, Huntington's disease, Parkinson's disease |
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. |
Synonyms: | AAC1; ANT; ANT 1; ANT1; MTDPS12; MTDPS12A; PEO2; PEO3; PEOA2; T1 |
Expression System: | HEK293 |
Formulation: | 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. |
Background: | The protein functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. |
Delivery: | In Stock |
Usage | Research use only |