Focal Adhesion Protein Antibody Kit

Focal Adhesion Protein Antibody Sampler Kit

Cat. Num. AAA2549973

• Applications: Western Blot
• Synonyms: Focal Adhesion Protein; Focal Adhesion Protein Antibody Sampler Kit; Focal Adhesion Protein antibody kit

• Applicable Applications for Focal Adhesion Protein antibody kit: Western Blot (WB)

Western Blot (WB)

(Western Blot analysis of HepG2 cells using FAK Polyclonal Antibody at dilution of 1:500.)

Western Blot (WB)

(Western Blot analysis of 293 cells with Paxillin Polyclonal Antibody.)

Western Blot (WB)

(Western Blot analysis of K562 cells using Talin-1 Polyclonal Antibody at dilution of 1:1000.)

Western Blot (WB)

(Western Blot analysis of A549, 3T3 cells using Tensin-2 Polyclonal Antibody at dilution of 1:500.)

Western Blot (WB)

(Western Blot analysis of Hela cells with Vinculin Polyclonal Antibody.)

Related Product Information for Focal Adhesion Protein antibody kit

Background/Introduction: FLICA is a powerful method to assess caspase activity. FLICA probes are cell permeant, noncytotoxic Fluorescent Labeled Inhibitors of CAspases that covalently bind to active caspase enzymes1, 2. Apoptosis is an evolutionarily conserved process of programmed cell death. It is centered on a cascade of proteolytic enzymes called caspases that are triggered in response to pro-apoptotic signals. Like the majority of other proteases, caspases are synthesized as pro-form precursors that undergo proteolytic maturation, either autocatalytically or in a cascade by enzymes with similar specificity3. Active caspase enzymes consist of two large (~20 kD) and two small (~10 kD) subunits that non-covalently associate to form a two heterodimer, tetrameric active caspase4. Once activated, caspases cleave protein substrates leading to the eventual disassembly of the cell. Caspases have been identified in organisms ranging from C. elegans to humans. Mammalian caspases play distinct roles in both apoptosis and inflammation. Mammalian caspase enzymes have been classified as initiator, executioner, and inflammatory caspases5. Once activated by initiator caspases (such as caspases-8,-9, and-10), executioner caspases-3 and/or-7 cleave specific sets of substrates that lead to apoptosis. Extrinsic activation of apoptosis, such as with FasL, TNF-a, or TRAIL binding to their associated death receptors, triggers the caspase-8 and-10-mediated cascade characteristic of the extrinsic apoptotic pathway, in which caspase-3 plays a dominant role6. In intrinsic apoptosis activation, DNA damage or inhibition of DNA repair leads to cytochrome c release from mitochondria, triggering formation of the apoptosome and activation of caspase-9. Once active, caspase-9 cleaves pro-form precusors of effector caspases, such as-3 and-7, leading to the eventual disassembly of the cell. FLICA 660 caspase-3/7 inhibitor probe contains the preferred binding sequence, Asp-Glu-Val-Asp (DEVD) for executioner caspases-3 and-7. This preferred caspase-3 and-7 binding sequence, DEVD, is labeled at the amino terminus end with a far-red fluorescent 660 dye and linked at the carboxyl end to a fluoromethyl ketone (FMK) reactive entity. The resulting cell permeant, fluorescent molecule, 660-DEVD-FMK, optimally excites at 660 nm and emits between 685-690 nm (Figure 1). A conventional red HeNe laser with a 633 nm excitation provides excellent excitation efficiency, enabling cells labeled with FLICA 660 to be analyzed with most flow cytometers, as well as fluorescence microscopes equipped with electronic grey scale image capabilities. To use FLICA, add it directly to the cell media, incubate, and wash. FLICA is cell-permeant and will efficiently diffuse in and out of all cells. If there is an active caspase-3 and/or-7 enzyme, it will covalently bind to FLICA 660-DEVD-FMK and retain the far-red fluorescent signal within the cell. Unbound FLICA will diffuse out of the cell during the wash steps. Apoptotic cells will retain a higher concentration of FLICA and fluoresce brighter than non-apoptotic cells. There is no interference from procaspases or inactive forms of the enzyme. If the treatment is causing cell death via apoptosis, apoptotic cells will have an elevated level of caspase-3/7 activity relative to non-apoptotic or negative control cells and fluoresce with FLICA. After labeling with FLICA, cells can be counterstained with other reagents and fixed or frozen.