Perforin (PRF1) (NM_005041) Human Recombinant Protein
CAT#: TP762413
Purified recombinant protein of Human perforin 1 (pore forming protein) (PRF1), transcript variant 1, Asp351-End, with N-terminal His tag, expressed in E.coli, 50ug
Other products for "PRF1"
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding the region (Asp351-End) of PRF1
|
Tag | N-His |
Predicted MW | 23.1 kDa |
Concentration | >50 ug/mL as determined by microplate BCA method |
Purity | >80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 50mM Tris, pH8.0, 8M Urea |
Storage | Store at -80°C after receiving vials. |
Stability | Stable for at least 1 year from receipt of products under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Reference Data | |
RefSeq | NP_005032 |
Locus ID | 5551 |
UniProt ID | P14222 |
Cytogenetics | 10q22.1 |
Refseq Size | 2512 |
Refseq ORF | 1665 |
Synonyms | HPLH2; P1; PFP |
Summary | 'This gene encodes a protein with structural similarities to complement component C9 that is important in immunity. This protein forms membrane pores that allow the release of granzymes and subsequent cytolysis of target cells. Whether pore formation occurs in the plasma membrane of target cells or in an endosomal membrane inside target cells is subject to debate. Mutations in this gene are associated with a variety of human disease including diabetes, multiple sclerosis, lymphomas, autoimmune lymphoproliferative syndrome (ALPS), aplastic anemia, and familial hemophagocytic lymphohistiocytosis type 2 (FHL2), a rare and lethal autosomal recessive disorder of early childhood. [provided by RefSeq, Aug 2017]' |
Protein Families | Druggable Genome |
Protein Pathways | Allograft rejection, Autoimmune thyroid disease, Graft-versus-host disease, Natural killer cell mediated cytotoxicity, Type I diabetes mellitus, Viral myocarditis |
Documents
FAQs |
SDS |
Resources
Recombinant Protein Resources |
{0} Product Review(s)
0 Product Review(s)
Submit review
Be the first one to submit a review
Product Citations
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen
complexities in the preparation of your product. International customers may expect an additional 1-2 weeks
in shipping.