- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Hsp27 (phospho S15) antibody (AB5581)
Immunocytochemistry/Immunofluorescence analysis of Hsp27 (phospho S15) (green) in HeLa cells either untreated (left) or treated with 10uM Anisomysin (right) for 30 minutes. Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% blocker BSA for 15 minutes at room temperature. Cells were incubated with ab5581 at 1 : 50 for at least 1 hour at room temperature, washed with PBS, and incubated with DyLight 488 goat anti-rabbit IgG secondary antibody (1 : 400) for 30 minutes at room temperature. F-Actin (red) was stained with DyLight 554 Phalloidin and nuclei (blue) were stained with Hoechst 33342 dye. 20X magnification.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Hsp27 (phospho S15) antibody (AB5581)
Immunocytochemistry analysis of Hsp27 using ab5581 at 2μg/mL concentration shows staining in 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized HeLa Cells treated with Anisomysin. The secondary antibody was Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, Alexa Fluor® 488 conjugate. Hsp27 (green), F-Actin staining with Alexa Fluor® 555 Rhodamine Phalloidin (red) and nuclei with SlowFade® Gold Antifade Mountant with DAPI (blue) is shown. Negative control has no primary antibody.
- IP
Supplier Data
Immunoprecipitation - Anti-Hsp27 (phospho S15) antibody (AB5581)
Immunoprecipitation of Hsp27 (phospho S15) was performed on HeLa cells treated with 10uM Anisomysin for 30 minutes. Antigen-antibody complexes were formed by incubating 500ug of whole cell lysate with 3ug of ab5581 overnight on a rocking platform at 4°C. The immune complexes were captured on 50ul Protein A/G Agarose, washed extensively, and eluted with Lane Marker Reducing Sample Buffer. Samples were then resolved on a 4-20% Tris-HCl polyacrylamide gel, transferred to a PVDF membrane, and blocked with 5% BSA/TBST for at least 1 hour. The membrane was probed with ab5581 at 1 : 500 overnight rotating at 4°C, washed with TBST, and probed with Clean-Blot IP Detection Reagent at 1/1000 for at least 1 hour. Chemiluminescent detection was performed using SuperSignal West Dura.
All lanes:
Immunoprecipitation - Anti-Hsp27 (phospho S15) antibody (ab5581)
Predicted band size: 23 kDa
false
- WB
Supplier Data
Western blot - Anti-Hsp27 (phospho S15) antibody (AB5581)
All lanes:
Western blot - Anti-Hsp27 (phospho S15) antibody (ab5581) at 1/500 dilution
Lane 1:
HeLa cell lysate - untreated at 50 µg
Lane 2:
HeLa cell lysate - treated with 10nM Anisomycin at 50 µg
Secondary
All lanes:
HRP-conjugated goat anti-rabbit IgG at 1/20000 dilution
Predicted band size: 23 kDa
false
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This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Hsp27 plays a critical role in cellular stress response by regulating actin cytoskeleton dynamics and inhibiting apoptosis. It forms part of a complex that includes other proteins such as alphaB-crystallin. This complex facilitates the reorganization of proteins under stress conditions enhancing cell survival during oxidative stress or thermal shock. Hsp27 also modulates inflammatory responses and has been shown to affect cell migration.
Pathways
Hsp27 integrates into the apoptosis and inflammation pathways. It interacts with apoptotic machinery such as caspase proteins to protect cells by hindering apoptosome formation. Additionally Hsp27 can engage with pathways involving the nuclear factor-kappa B (NF-kB) impacting inflammatory signaling. CPTC (carboxyl-pyrene-trioctylamine) can modulate these pathways by altering Hsp27 function and interactions.
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Journal of animal science 101: PubMed37688555
2023
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Nature cell biology 25:467-480 PubMed36690850
2023
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International journal of molecular sciences 23: PubMed36499735
2022
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Journal of ophthalmology 2021:4668056 PubMed35154818
2021
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Molecular medicine reports 12:3787-3794 PubMed26044344
2015
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BMC neuroscience 6:24 PubMed15819993
2005
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