Recombinant Human Peroxiredoxin 6/PRDX6 Protein (His Tag) (PKSH031178)
For research use only.
| Synonyms | 1-Cys PRX, 1-Cys Peroxiredoxin, 24 kDa Protein, AOP2, Acidic Calcium-Independent Phospholipase A2, Antioxidant Protein 2, KIAA0106, Liver 2D PAGE Spot 40, NSGPx, Non-Selenium Glutathione Peroxidase, PRDX6, Peroxiredoxin-6, Red Blood Cells Page Spot 12, aiPLA2, p29 |
| Species | Human |
| Expression Host | E.coli |
| Sequence | Met 1-Pro 224 |
| Accession | P30041 |
| Calculated Molecular Weight | 26.5 kDa |
| Observed Molecular Weight | 26.5 kDa |
| Tag | N-His |
| Bio-activity | Not validated for activity |
| Purity | > 95 % as determined by reducing SDS-PAGE. |
| Endotoxin | Please contact us for more information. |
| Storage | Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months. |
| Shipping | This product is provided as lyophilized powder which is shipped with ice packs. |
| Formulation |
Lyophilized from sterile PBS, pH 7.4 Normally 5% - 8% trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization. Please refer to the specific buffer information in the printed manual. |
| Reconstitution | Please refer to the printed manual for detailed information. |
| Background | acid phosphatase-like protein 2; also known as ACPL2; is a secreted protein which belongs to thehistidine acid phosphatase family. A large-scale effort; termed the Secreted Protein Discovery Initiative (SPDI); was undertaken to identify novel secreted and transmembrane proteins. In the first of several approaches; a biological signal sequence trap in yeast cells was utilized to identify cDNA clones encoding putative secreted proteins. A second strategy utilized various algorithms that recognize features such as the hydrophobic properties of signal sequences to identify putative proteins encoded by expressed sequence tags (ESTs) from human cDNA libraries. A third approach surveyed ESTs for protein sequence similarity to a set of known receptors and their ligands with the BLAST algorithm. Finally; both signal-sequence prediction algorithms and BLAST were used to identify single exons of potential genes from within human genomic sequence. |
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