SNX27 (NM_030918) Human Mass Spec Standard
Specifications
| Product Data | |
| Tag | C-Myc/DDK |
|---|---|
| Species | Human |
| Expression Host | HEK293 |
| Expression cDNA Clone or AA Sequence | RC218477 |
| Predicted MW | 59.6 kDa |
| Protein Sequence | |
| Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
| Concentration | >0.05 µg/µL as determined by microplate BCA method |
| Labeling Method | Labeled with U- 13C6, 15N4-L-Arginine and U- 13C6, 15N2-L-Lysine |
| Buffer | 25 mM Tris-HCl, 100 mM glycine, pH 7.3 |
| Storage | Store at -80°C. Avoid repeated freeze-thaw cycles. |
| Stability | Stable for 3 months from receipt of products under proper storage and handling conditions. |
| Shipping | Dry Ice |
| Reference Data | |
| RefSeq | NP_112180 |
| RefSeq Size | 7085 |
| RefSeq ORF | 1584 |
| Synonyms | MRT1; MY014 |
| Locus ID | 81609 |
| UniProt ID | Q96L92 |
| Cytogenetics | 1q21.3 |
| Summary | This gene encodes a member of the sorting nexin family, a diverse group of cytoplasmic and membrane-associated proteins involved in endocytosis of plasma membrane receptors and protein trafficking through these compartments. All members of this protein family contain a phosphoinositide binding domain (PX domain). A highly similar protein in mouse is responsible for the specific recruitment of an isoform of serotonin 5-hydroxytryptamine 4 receptor into early endosomes, suggesting the analogous role for the human protein. provided by RefSeq, Jul 2008 |
Reviews
Documents
| FAQs |
| SDS |
Resources
| Recombinant Protein Resources |
Other "SNX27" proteins (3)
| SKU | Description | Size | Price | |
|---|---|---|---|---|
| LC403094 | Lyophilized SNX27 HEK293T cell transient overexpression lysate (as WB positive control) | 20 ug |
$206.00
|
|
| LY403094 | Transient overexpression lysate of sorting nexin family member 27 (SNX27) (as WB positive control) | 100 ug |
$665.00
|
|
| TP318477 | Recombinant protein of human sorting nexin family member 27 (SNX27), 20 µg | 20 ug |
$737.00
|
|
Citations
Loo, Tang, Al-Haddawi et al
Nat Commun (2014) 5, 3176 DOI: 10.1038/ncomms4176
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