Rabbit Polyclonal FLASH antibody. Suitable for WB, ICC/IF and reacts with Human samples. Cited in 2 publications. Immunogen corresponding to Synthetic Peptide within Human CASP8AP2 aa 1950 to C-terminus.
pH: 7.2
Preservative: 0.02% Sodium azide
WB | ICC/IF | |
---|---|---|
Human | Tested | Tested |
Mouse | Predicted | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.25000-0.50000 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 10 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes - |
Participates in TNF-alpha-induced blockade of glucocorticoid receptor (GR) transactivation at the nuclear receptor coactivator level, upstream and independently of NF-kappa-B. Suppresses both NCOA2- and NCOA3-induced enhancement of GR transactivation. Involved in TNF-alpha-induced activation of NF-kappa-B via a TRAF2-dependent pathway. Acts as a downstream mediator for CASP8-induced activation of NF-kappa-B. Required for the activation of CASP8 in FAS-mediated apoptosis. Required for histone gene transcription and progression through S phase.
FLASH, KIAA1315, RIP25, CASP8AP2, CASP8-associated protein 2, FLICE-associated huge protein
Rabbit Polyclonal FLASH antibody. Suitable for WB, ICC/IF and reacts with Human samples. Cited in 2 publications. Immunogen corresponding to Synthetic Peptide within Human CASP8AP2 aa 1950 to C-terminus.
pH: 7.2
Preservative: 0.02% Sodium azide
A novel mammalian CED-4 homologous was recently identified and cloned in mouse (1) and human (2) and designated FLASH (for FLICE-associated huge protein). FLASH is involved in Fas induced apoptosis. It is recruited to Fas after the receptor cross-linking. Overexpression of wild type of FLASH facilitates and its dominant negative form inhibits Fas induced apoptosis. FLASH interacts with the DEDs of caspase-8 and FADD through the DED-like domain of FLASH and mediates activation of caspase-8 (1). There are parallels between FLASH and Apaf-1/CED-4 although there are arguments against their structural similarity (1,2).
FLASH also known as "CASP8 and FADD-like apoptosis regulator" is an important protein that plays a role in apoptosis. This protein has a molecular mass of approximately 220 kDa and can be found expressed in various tissues including the liver kidney and heart. FLASH localizes to the nucleus where it interacts with several nuclear components and contributes to critical cellular functions. Researchers recognize its significance in regulating apoptotic pathways making it a target for studies involving cell death.
The CASP8 and FADD-like apoptosis regulator is part of the complex involved in the regulation of apoptosis and cell cycle. FLASH plays its part by interacting with other apoptotic factors ensuring proper cell cycle progression and programmed cell death. It associates with the death effector domain (DED) proteins and has shown involvement in the activation of caspase-8. This regulation is significant for maintaining cellular homeostasis and preventing the development of cancerous cells.
Studies show that FLASH integrates into the apoptotic pathway and NF-kB signaling cascade. It engages in critical interactions with proteins such as FADD and caspase-8 which are essential for the initiation and execution of apoptosis. By influencing NF-kB signaling FLASH modulates inflammatory responses and survival signals effectively balancing cell death and survival mechanisms.
Research frequently connects FLASH to cancer and autoimmune diseases. Its dysregulation can lead to aberrant apoptotic signaling contributing to cancer progression or inappropriate cell death as seen in autoimmune conditions. FLASH’s interaction with proteins like caspase-8 makes it an attractive target for developing therapies for diseases where apoptosis is disrupted. Understanding FLASH’s function and interactions provides insight into potential therapeutic strategies.
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All lanes: Western blot - Anti-FLASH antibody (ab8420) at 0.5 µg/mL
All lanes: HeLa whole cell lysate
Predicted band size: 223 kDa
Observed band size: 220 kDa
ab8420 at 10μg/ml staining FLASH in Hela cells by ICC/IF
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