RIPK1/RIP1 Products
RIPK1 (Receptor (TNFRSF)-Interacting Serine-Threonine Kinase 1), also known as RIP1, contains an N-terminal protein kinase domain, a C-terminal death domain, and a unique internal region called the intermediate domain. It is a serine/threonine protein kinase and is constitutively expressed in many tissues. RIPK1 interacts with the cytoplasmic death domain of FAS and TNF receptors, and is an important element in apoptotic processes. RIPK1 has been shown to interact with a number of proteins including TRADD, TRAF1, TRAF2, and TRAF3, to form larger signaling complexes. These complexes, in turn, activate specific signaling cascades, such as NFkB.
6 results for "RIPK1/RIP1" in Products
Search
Application
Product Action
Conjugates
Clonality
Isotype
Clone
Low Endotoxin
Sample Size
Citations
Reviews
RIPK1/RIP1 Products
RIPK1 (Receptor (TNFRSF)-Interacting Serine-Threonine Kinase 1), also known as RIP1, contains an N-terminal protein kinase domain, a C-terminal death domain, and a unique internal region called the intermediate domain. It is a serine/threonine protein kinase and is constitutively expressed in many tissues. RIPK1 interacts with the cytoplasmic death domain of FAS and TNF receptors, and is an important element in apoptotic processes. RIPK1 has been shown to interact with a number of proteins including TRADD, TRAF1, TRAF2, and TRAF3, to form larger signaling complexes. These complexes, in turn, activate specific signaling cascades, such as NFkB.
6 results for "RIPK1/RIP1" in Products
Clonality : | Monoclonal |
Host : | Mouse IgG1 Clone #334640 |
Applications : | Immunocytochemistry/Immunofluorescence, Knockout Validated, Simple Western, Western Blot |
Contains 4 membranes-each spotted in duplicate with 49 different antibodies to ubiquitin target proteins
RIP1 kinase inhibitor; inhibits necroptosis
Chemical Name : | 5-(1H-Indol-3-ylmethyl)-3-methyl-2-thioxo-4-imidazolidinone |
Purity : | ≥98% (HPLC) |
Necroptosis inhibitor; also inhibits pyroptosis
Chemical Name : | (2E)-N-[4-[[(3-Methoxy-2-pyrazinyl)amino]sulfonyl]phenyl]-3-(5-nitro-2-thienyl)-2-propenamide |
Purity : | ≥98% (HPLC) |
Potent and metabolically stable RIP1 kinase inhibitor
Chemical Name : | N-Hydroxy-2,2-dimethyl-N-(phenylmethyl)butanamide |
Purity : | ≥98% (HPLC) |