FGR overexpression 293T lysate (whole cell) suitable for WB. View our extensive range of validated lysates from normal and diseased human, mouse and rat tissue.
FGR_HUMAN, FLJ43153, Gardner Rasheed feline sarcoma viral (v fgr), Gardner-Rasheed feline sarcoma viral (v-fgr) oncogene homolog, MGC75096, P55-FGR, Proto oncogene tyrosine protein kinase FGR, Proto-oncogene c-Fgr, SRC 2, Tyrosine-protein kinase Fgr, c fgr, c fgr protooncogene, c src 2 proto oncogene, c src2, p55 c fgr protein, p55c fgr, p58-Fgr, p58c-Fgr
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FGR overexpression 293T lysate (whole cell) suitable for WB. View our extensive range of validated lysates from normal and diseased human, mouse and rat tissue.
ab94154 is a 293T cell transfected lysate in which Human FGR has been transiently over-expressed using a pCMV-FGR plasmid. The lysate is provided in 1X Sample Buffer.
The FGR protein also known as Src-like adapter protein or FGR proto-oncogene is an important cellular component with a mass of approximately 58 kDa. Expressed mainly in hematopoietic cells like macrophages and neutrophils the FGR protein belongs to the Src family of non-receptor tyrosine kinases. This protein has the ability to modulate various cellular processes through its kinase activity influencing the phosphorylation of substrates involved in signal transduction.
The FGR protein impacts processes related to immune responses and cell communication. It participates in the formation of multi-protein complexes enabling interactions that mediate pathways important for cellular signaling. Through these interactions the FGR protein controls important processes like cell growth differentiation and movement especially in immune cell types. Its role in signal transduction renders it a critical player in various immune functions.
The FGR protein integrates into the signaling networks such as the MAPK/ERK pathway and PI3K/AKT pathway which are pivotal for cell survival and proliferation. Within these pathways FGR interacts with other proteins like the GRB2 and PI3K to mediate downstream effects that influence many cellular responses. These interactions ensure that alterations in external signals lead to appropriate cellular outcomes sustaining a balance in cellular behavior and immune functions.
Alterations in the expression or mutation of the FGR protein have associations with certain cancers and inflammatory diseases. Enhanced FGR activity has been observed in specific leukemia cases where its interaction with proteins like ABL1 and BCR-ABL1 contributes to oncogenic processes. Similarly abnormalities in FGR signaling pathways can result in immune dysfunctions implicating proteins like Lyn and Hck in pathologies such as rheumatoid arthritis. Understanding the role of FGR within disease contexts aids in identifying therapeutic targets for these conditions.
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ab94154 at 15µg/lane on an SDS-PAGE gel.
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