Your Position: Home
> Leukemia Therapeutic Targets Leukemia Therapeutic Targets
| Protein Name | Alternative Names | BioChemical Class / Role | Products (Cat NO)![]() |
||
| Protein | Antibody | Gene cDNA clones | |||
| CD116/GM-CSFR | Csfgmra, GM-CSF-Ra, Csf2ra | The granulocyte macrophage colony-stimulating factor receptor (GM-CSFR) also known as CD116, is a low affinity receptor for granulocyte macrophage colony-stimulating factor (GM-CSF), which stimulates the production of white blood cells. The CD116/GM-CSFR is a heterodimer composed of at least two different subunits, an α chain, and a β chain which is also present in the receptors for IL-3 and IL-5. | 10701-H02H, 10701-H08H | HG10701-M | |
| Mcl-1 | HG10240-M | ||||
| PLK1/PLK-1 | STPK13 | Serine/threonine-protein kinase PLK1, also known as Polo-like kinase 1, PLK1 and STPK13, is a member protein kinase superfamily and CDC5/Polo subfamily. Studies have shown that the loss of PLK1 expression can induce pro-apoptotic pathways and inhibit growth. Moreover, PLK1 seems to be involved in the tumor suppressor p53 related pathways. Evidence suggests that PLK1 can inhibit transactivation and pro-apoptotic functions of p53 function by physical interaction and phosphorylation. | 10676-H07B | HG10676-M | |
| CDK9/CDC2L4 | HG10907-M | ||||
| Leukotriene A4 Hydrolase/LTA4H | As a bifunctional zinc metalloenzyme, LTA4H also exhibits an anion-dependant arginyl aminopeptidase activity of high efficiency and specificity in addition to its epoxide hydrolase activity. This enzyme belongs to the family of hydrolases, specifically those acting on ether bonds (ether hydrolases). LTA4H participates in arachidonic acid metabolism, and is regarded as a therapeutic target for inflammation. | 10276-H08B | HG10276-M, MG50268-M | ||
| PKC alpha | HG10026-M | ||||
| JAK2 | HG11198-M | ||||
| VEGFR1/FLT-1 | FLT1, FLT | HG10136-M | |||
| VEGFR2/Flk-1/CD309 | KDR, VEGFR | A vascular endothelial growth factor (VEGF) receptor. | 10012-H02H | HG10012-M | |
| VEGFR3/FLT-4 | FLT41, LMPH1A, PCL | VEGFR3 (FLT-4), together with the other two members VEGFR1 (FLT-1) and VEGF R2 (KDR/Flk-1) are receptors for vascular endothelial growth factors (VEGF) and belong to the class III subfamily of receptor tyrosine kinases (RTKs). | 10806-H02H, 10806-H08H | 10806-MM02, 10806-MM03, 10806-RP01, 10806-RP04 | HG10806-M |
| MMP-1/MMP1 | CLG, CLGN | HG10532-M | |||
| MMP-2/MMP2 | CLG4, CLG4A, MMP-II, MONA, TBE-1 | HG10082-M | |||
| MMP-3/MMP3 | CHDS6, MGC126102, MGC126103, MGC126104, MMP-3, SL-1, STMY, STMY1, STR1 | HG10467-M | |||
| MMP-7/MMP7 | MPSL1, PUMP-1 | MMP7, also referred to as matrilysin, is the smallest member of the MMP family and differs from other MMP members in that it lacks the C-terminal hemopexin-like domain. This enzyme serves essential functions in both innate defense and wound healing, and appears to be one of the most important MMPs in human colon cancers. In addition, matrilysin is also identified as a mediator of pulmonary fibrosis and a potential therapeutic target. | 10277-H01H | HG10277-M | |
| MMP-8/MMP8 | CLG1, HNC, PMNL-CL | HG10254-M | |||
| MMP-9/MMP9 | CLG4B, GELB, MANDP2 | MMP9, also known as 92-kDa gelatinase B/type IV collagenase, is secreted from neutrophils, macrophages. This enzyme degrades various substrates including gelatin, collagen types IV and V, and elastin. MMP9 is involved in a variety of autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis, and multiple sclerosis, and be regarded as a potential therapeutic target. | 10327-H08H, 10327-HNAE | 10327-MM01, 10327-MM02, 10327-RM04, 10327-RM05, 10327-RP03, 10327-RP06 | HG10327-M |
| MMP-10/MMP10 | SL-2, STMY2 | HG10249-M | |||
| MMP-12/MMP12 | HME, MGC138506, MME | HG10266-M | |||
| MMP-14/MMP14 | MMP-X1, MTMMP1, MT1-MMP | HG10741-M | |||
| CDKN1A | CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 | HG11108-M | |||
| SGK1/SGK | HG10543-M, MG50278-M | ||||
+86-400-890-9989




