ARG44030
anti-Perforin antibody [dG9] (APC)
anti-Perforin antibody [dG9] (APC) for Flow cytometry and Human
Overview
Product Description | APC-conjugated Mouse Monoclonal antibody [dG9] human Perforin |
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Tested Reactivity | Hu |
Tested Application | FACS |
Host | Mouse |
Clonality | Monoclonal |
Clone | dG9 |
Isotype | IgG2b, kappa |
Target Name | Perforin |
Antigen Species | Human |
Immunogen | Human YT lymphoma cell line |
Conjugation | APC |
Protein Full Name | Perforin-1 |
Alternate Names | PRF1; Perforin 1; PFP; P1; HPLH2; Perforin 1 (Pore Forming Protein); Lymphocyte Pore-Forming Protein; Perforin-1; Cytolysin; Perforin 1 (Preforming Protein); Perforin |
Application Instructions
Application Suggestion |
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Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
Form | Liquid |
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Purification | Purified |
Buffer | PBS (pH 7.4) and 15 mM Sodium azide. |
Preservative | 15 mM Sodium azide |
Storage Instruction | Aliquot and store in the dark at 2-8°C. Keep protected from prolonged exposure to light. Do not freeze. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
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Gene Symbol | PRF1 |
Gene Full Name | Perforin 1 |
Background | 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. |
Function | Pore-forming protein that plays a key role in granzyme-mediated programmed cell death, and in defense against virus-infected or neoplastic cells. |
Cellular Localization | Cell membrane, Endosome, Lysosome, Membrane, Secreted |
PTM | Disulfide bond, Glycoprotein |
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