Monoclonal Antibody to Caspase-8 (Clone: ABM14C1)

Fig-1:Western blot analysis of Caspase-8. Anti-Caspase-8 antibody (Clone: ABM14C1) was used at 2 µg/ml on Molt-4, Kato III and HepG2 lysates.

Monoclonal Antibody to Caspase-8 (Clone: ABM14C1)

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Fig-1:Western blot analysis of Caspase-8. Anti-Caspase-8 antibody (Clone: ABM14C1) was used at 2 µg/ml on Molt-4, Kato III and HepG2 lysates.

Fig-2: Intracellular Flow analysis of Caspase-8 antibody in Hela cells using 0.5 µg/ 10^6 cells of anti-Caspase-8 antibody (ABM14C1). Green represents isotype control; red represents anti-Caspase-8 antibody. Goat anti-mouse PE conjugate was used as secondary antibody. (Cells were fixed with 4% paraformaldehyde for 10 min and washed with PBS by centrifuging at 1100 for 5 min followed by permeabilization for 20 min and washed again as mentioned above. Then cell were incubated with primary antibody for 45 min. and after washing the cells twice in PBS, incubated with conjugated secondary antibody for 30 min. Data acquisition was done after washing twice with PBS as mentioned above).

Fig-3: Intracellular Flow analysis of Caspase-8 antibody in Jurkat cells using 0.5 µg/ 10^6 cells of anti-Caspase-8 antibody (ABM14C1). Green represents isotype control; red represents anti-Caspase-8 antibody. Goat anti-mouse PE conjugate was used as secondary antibody. (Cells were fixed with 4% paraformaldehyde for 10 min and washed with PBS by centrifuging at 1100 for 5 min followed by permeabilization for 20 min and washed again as mentioned above. Then cell were incubated with primary antibody for 45 min. and after washing the cells twice in PBS, incubated with conjugated secondary antibody for 30 min. Data acquisition was done after washing twice with PBS as mentioned above).

Fig-4: Immunohistochemical analysis of Caspase-8 in human Esophagus using anti-Caspase-8 antibody (Clone: ABM14C1) at 5 µg/ml.

Fig-5: Immunohistochemical analysis of Caspase-8 in human Tonsil using anti-Caspase-8 antibody (Clone: ABM14C1) at 5 µg/ml.

Figure-6: Western blot analysis of Caspase-8. Anti-Caspase-8 antibody (Clone: ABM14C1) was used at 4 µg/ml on EL-4 lysate.

Product code: 10-1019

Clone name :	ABM14C1
Clonality :	Monoclonal
Application :	IHC, FACS, WB
Reactivity :	Mouse, Human

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Format :	Purified
Amount :	100 µg
Isotype :	Mouse IgG1
Purification :	Protein G Chromatography
Content :	25 µg in 50 µl/100 µg in 200 µl PBS containing 0.05% BSA and 0.05% sodium azide. Sodium azide is highly toxic.
Storage condition :	Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.


Gene :	CASP8
Gene ID :	841
Uniprot ID :	Q14790
Alternative Name :	Apoptotic cysteine protease, Apoptotic protease Mch-5, FADD-homologous ICE/ced-3-like protease, CE-like apoptotic protease 5
Immunogen Information :	A partial length recombinant protein (a.a 179-385) of Caspase-8 was used as the immunogen for this antibody.

Apoptosis occurs during normal cellular development and involves dramatic changes in cellular structure. Disruption of apoptosis may contribute to cancer as well as other autoimmune diseases. Caspase family of cysteine proteases has been shown to play a key role in apoptosis. Caspase-8 is a 55 kDa cytosolic protein that is synthesized as an inactive pro-enzyme. Activation of caspase-8 involves a two-step proteolysis: the cleavage of caspase-8 to generate a 43 and a 12 kDa fragment which is further processed to 10 kDa. The p43 is then cleaved to yield p26 and the release of the active site containing p18.The Active/Cleaved Caspase-8 polyclonal antisera recognizes the large and small subunits of active/cleaved caspase-8. Whereas the antisera has a strong preference for active/cleaved caspase-8, in some cell or tissue systems or techniques the antisera may also recognize the proform of caspase-8 as well as intermediate caspase-8 cleavage fragments.

WB: 4-6 µg/ml, FACS: 0.5-1 µg/10^6, IHC: 5-10 µg/ml

For Research Use Only. Not for use in diagnostic/therapeutics procedures.

Nidhi Varshney1, Dharmendra Kashyap1, Vaishali Saini1, Siddharth Singh1, Sachin Kumar2, Manivannan Elangovan3, NatÃ©rcia F. BrÃ¡s4, Hem Chandra Jha1
Unveiling the therapeutic potential of Ponatinib and Imatinib against Aurora Kinase A in gastric cancer cells https://doi.org/10.21203/rs.3.rs-3195156/v1

Subcellular location:	Cytoplasm
Post transnational modification:	Phosphorylation on Ser-387 during mitosis by CDK1 inhibits activation by proteolysis and prevents apoptosis. This phosphorylation occurs in cancer cell lines, as well as in primary breast tissues and lymphocytes.
Tissue Specificity:	Isoform 1, isoform 5 and isoform 7 are expressed in a wide variety of tissues. Highest expression in peripheral blood leukocytes, spleen, thymus and liver. Barely detectable in brain, testis and skeletal muscle.
BioGrid:	107291. 153 interactions.