p hsp27 Search Results


p hsp27  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology p hsp27
Schematic model representing the regulation of actin stress fibers and focal adhesions by ER. The model shows activation of a signaling cascade that involves ER interaction with α2β1, activation of cAMP, PKA, and FAK, followed by the transient activation of p38 MAPK and <t>Hsp27,</t> and ultimately disassembly of actin stress fibers and focal adhesions. The various blocking agents are also illustrated. For additional details see the text.
P Hsp27, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p+hsp27/p-HSP+27+Antibody/pmc02172143-220-21-22
Average 93 stars, based on 1 article reviews
p hsp27 - by Bioz Stars, 2026-10
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human hsp27  (R&D Systems)
86
R&D Systems human hsp27
Heat-shock protein 27 <t>(Hsp27)</t> is associated with LYM resistance to DOX and decreased HLA-DR expression on monocytes. (A) LYM co-cultured with monocytes with and without DOX have increased intracellular Hsp27 expression . Quantitative analysis of LYM (Granta-519) intracellular Hsp27 expression by immunoblot is shown (mean ± SD, n = 3). Representative immunoblot images are shown above each condition. (B) Quantitative analysis of LYM intracellular Hsp27 expression by flow cytometry is shown for OCI-Ly3 ( n = 4) and OCI-Ly10 ( n = 6; mean ± SD). Representative histogram of OCI-Ly3 intracellular Hsp27 expression are shown above the corresponding condition (shaded = isotype control; line = Hsp27). (C) Hsp27 can directly induce decreased HLA-DR expression on monocytes in a dose-dependent manner (left panel, n = 4). LYM cells can secrete Hsp27 . Supernatants from LYM cells and monocyte co-culture with and without DOX have significantly higher soluble Hsp27 compared to media (right panel, white bars, left axis). Culture supernatant from LYM co-culture high in Hsp27, but not media or supernatant from normal B cell co-culture, induced decreased HLA-DR expression on normal CD14 + HLA-DR + monocytes (right panel, black bars, right axis: LYM = Granta-519; n = 6; * p < 0.05 compared to control media; Δ p < 0.05 compared to normal B cell and monocyte co-culture supernatant.) (D) More importantly, Hsp27 is detectable in plasma of patients with lymphoma. Increased plasma level of Hsp27 correlated with increased percentage of CD14 + HLA-DR low/neg monocytes in blood (left panel). Patients who were refractory to DOX treatments had higher plasma Hsp27 levels than those who responded to treatments (right panel).
Human Hsp27, supplied by R&D Systems, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p+hsp27/Human+HSP27+%5Bp+Ser15%5D+ELISA+Kit+(Colorimetric)/pmc04485750-149-4-6
Average 86 stars, based on 1 article reviews
human hsp27 - by Bioz Stars, 2026-10
86/100 stars
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phosphorylated heat shock protein 27 (p-hsp27) analysis  (Confluence Discovery Technologies)
90
Confluence Discovery Technologies phosphorylated heat shock protein 27 (p-hsp27) analysis
Heat-shock protein 27 <t>(Hsp27)</t> is associated with LYM resistance to DOX and decreased HLA-DR expression on monocytes. (A) LYM co-cultured with monocytes with and without DOX have increased intracellular Hsp27 expression . Quantitative analysis of LYM (Granta-519) intracellular Hsp27 expression by immunoblot is shown (mean ± SD, n = 3). Representative immunoblot images are shown above each condition. (B) Quantitative analysis of LYM intracellular Hsp27 expression by flow cytometry is shown for OCI-Ly3 ( n = 4) and OCI-Ly10 ( n = 6; mean ± SD). Representative histogram of OCI-Ly3 intracellular Hsp27 expression are shown above the corresponding condition (shaded = isotype control; line = Hsp27). (C) Hsp27 can directly induce decreased HLA-DR expression on monocytes in a dose-dependent manner (left panel, n = 4). LYM cells can secrete Hsp27 . Supernatants from LYM cells and monocyte co-culture with and without DOX have significantly higher soluble Hsp27 compared to media (right panel, white bars, left axis). Culture supernatant from LYM co-culture high in Hsp27, but not media or supernatant from normal B cell co-culture, induced decreased HLA-DR expression on normal CD14 + HLA-DR + monocytes (right panel, black bars, right axis: LYM = Granta-519; n = 6; * p < 0.05 compared to control media; Δ p < 0.05 compared to normal B cell and monocyte co-culture supernatant.) (D) More importantly, Hsp27 is detectable in plasma of patients with lymphoma. Increased plasma level of Hsp27 correlated with increased percentage of CD14 + HLA-DR low/neg monocytes in blood (left panel). Patients who were refractory to DOX treatments had higher plasma Hsp27 levels than those who responded to treatments (right panel).
Phosphorylated Heat Shock Protein 27 (P Hsp27) Analysis, supplied by Confluence Discovery Technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p+hsp27/phosphorylated+heat+shock+protein+27++p+hsp27++analysis/pmc08203602-115-19-4
Average 90 stars, based on 1 article reviews
phosphorylated heat shock protein 27 (p-hsp27) analysis - by Bioz Stars, 2026-10
90/100 stars
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rabbit-anti-human phosphorylated-(p-)hsp27 antibody  (Bioworld Antibodies)
90
Bioworld Antibodies rabbit-anti-human phosphorylated-(p-)hsp27 antibody
Heat-shock protein 27 <t>(Hsp27)</t> is associated with LYM resistance to DOX and decreased HLA-DR expression on monocytes. (A) LYM co-cultured with monocytes with and without DOX have increased intracellular Hsp27 expression . Quantitative analysis of LYM (Granta-519) intracellular Hsp27 expression by immunoblot is shown (mean ± SD, n = 3). Representative immunoblot images are shown above each condition. (B) Quantitative analysis of LYM intracellular Hsp27 expression by flow cytometry is shown for OCI-Ly3 ( n = 4) and OCI-Ly10 ( n = 6; mean ± SD). Representative histogram of OCI-Ly3 intracellular Hsp27 expression are shown above the corresponding condition (shaded = isotype control; line = Hsp27). (C) Hsp27 can directly induce decreased HLA-DR expression on monocytes in a dose-dependent manner (left panel, n = 4). LYM cells can secrete Hsp27 . Supernatants from LYM cells and monocyte co-culture with and without DOX have significantly higher soluble Hsp27 compared to media (right panel, white bars, left axis). Culture supernatant from LYM co-culture high in Hsp27, but not media or supernatant from normal B cell co-culture, induced decreased HLA-DR expression on normal CD14 + HLA-DR + monocytes (right panel, black bars, right axis: LYM = Granta-519; n = 6; * p < 0.05 compared to control media; Δ p < 0.05 compared to normal B cell and monocyte co-culture supernatant.) (D) More importantly, Hsp27 is detectable in plasma of patients with lymphoma. Increased plasma level of Hsp27 correlated with increased percentage of CD14 + HLA-DR low/neg monocytes in blood (left panel). Patients who were refractory to DOX treatments had higher plasma Hsp27 levels than those who responded to treatments (right panel).
Rabbit Anti Human Phosphorylated (P )Hsp27 Antibody, supplied by Bioworld Antibodies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p+hsp27/p+hsp27++ser15+antibody/pm25373458-56-9-13
Average 90 stars, based on 1 article reviews
rabbit-anti-human phosphorylated-(p-)hsp27 antibody - by Bioz Stars, 2026-10
90/100 stars
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anti phospho hsp27  (R&D Systems)
86
R&D Systems anti phospho hsp27
Heat-shock protein 27 <t>(Hsp27)</t> is associated with LYM resistance to DOX and decreased HLA-DR expression on monocytes. (A) LYM co-cultured with monocytes with and without DOX have increased intracellular Hsp27 expression . Quantitative analysis of LYM (Granta-519) intracellular Hsp27 expression by immunoblot is shown (mean ± SD, n = 3). Representative immunoblot images are shown above each condition. (B) Quantitative analysis of LYM intracellular Hsp27 expression by flow cytometry is shown for OCI-Ly3 ( n = 4) and OCI-Ly10 ( n = 6; mean ± SD). Representative histogram of OCI-Ly3 intracellular Hsp27 expression are shown above the corresponding condition (shaded = isotype control; line = Hsp27). (C) Hsp27 can directly induce decreased HLA-DR expression on monocytes in a dose-dependent manner (left panel, n = 4). LYM cells can secrete Hsp27 . Supernatants from LYM cells and monocyte co-culture with and without DOX have significantly higher soluble Hsp27 compared to media (right panel, white bars, left axis). Culture supernatant from LYM co-culture high in Hsp27, but not media or supernatant from normal B cell co-culture, induced decreased HLA-DR expression on normal CD14 + HLA-DR + monocytes (right panel, black bars, right axis: LYM = Granta-519; n = 6; * p < 0.05 compared to control media; Δ p < 0.05 compared to normal B cell and monocyte co-culture supernatant.) (D) More importantly, Hsp27 is detectable in plasma of patients with lymphoma. Increased plasma level of Hsp27 correlated with increased percentage of CD14 + HLA-DR low/neg monocytes in blood (left panel). Patients who were refractory to DOX treatments had higher plasma Hsp27 levels than those who responded to treatments (right panel).
Anti Phospho Hsp27, supplied by R&D Systems, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p+hsp27/HSP27+%5Bp+Ser82%5D+Antibody+(GT357)/pm17577736-80-38-43
Average 86 stars, based on 1 article reviews
anti phospho hsp27 - by Bioz Stars, 2026-10
86/100 stars
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p hsp27 actin interaction  (Cold Spring Harbor Laboratory Meetings)
86
Cold Spring Harbor Laboratory Meetings p hsp27 actin interaction
Heat-shock protein 27 <t>(Hsp27)</t> is associated with LYM resistance to DOX and decreased HLA-DR expression on monocytes. (A) LYM co-cultured with monocytes with and without DOX have increased intracellular Hsp27 expression . Quantitative analysis of LYM (Granta-519) intracellular Hsp27 expression by immunoblot is shown (mean ± SD, n = 3). Representative immunoblot images are shown above each condition. (B) Quantitative analysis of LYM intracellular Hsp27 expression by flow cytometry is shown for OCI-Ly3 ( n = 4) and OCI-Ly10 ( n = 6; mean ± SD). Representative histogram of OCI-Ly3 intracellular Hsp27 expression are shown above the corresponding condition (shaded = isotype control; line = Hsp27). (C) Hsp27 can directly induce decreased HLA-DR expression on monocytes in a dose-dependent manner (left panel, n = 4). LYM cells can secrete Hsp27 . Supernatants from LYM cells and monocyte co-culture with and without DOX have significantly higher soluble Hsp27 compared to media (right panel, white bars, left axis). Culture supernatant from LYM co-culture high in Hsp27, but not media or supernatant from normal B cell co-culture, induced decreased HLA-DR expression on normal CD14 + HLA-DR + monocytes (right panel, black bars, right axis: LYM = Granta-519; n = 6; * p < 0.05 compared to control media; Δ p < 0.05 compared to normal B cell and monocyte co-culture supernatant.) (D) More importantly, Hsp27 is detectable in plasma of patients with lymphoma. Increased plasma level of Hsp27 correlated with increased percentage of CD14 + HLA-DR low/neg monocytes in blood (left panel). Patients who were refractory to DOX treatments had higher plasma Hsp27 levels than those who responded to treatments (right panel).
P Hsp27 Actin Interaction, supplied by Cold Spring Harbor Laboratory Meetings, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p+hsp27/actin+hsp27+interaction+p/10__18066_slash_revistaunivap__v25i48__2259-250-10-0
Average 86 stars, based on 1 article reviews
p hsp27 actin interaction - by Bioz Stars, 2026-10
86/100 stars
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hsp27 [p ser78] antibody (2079a) [alexa fluor® 350]  (Novus Biologicals)
N/A
The HSP27 [p Ser78] Antibody (2079A) [Alexa Fluor® 350] from Novus is a HSP27 antibody to HSP27. This antibody reacts with Human. The HSP27 antibody has been validated for the following applications: Western Blot, Flow
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hsp27 [p ser78] antibody (2079a) [alexa fluor® 532]  (Novus Biologicals)
N/A
The HSP27 [p Ser78] Antibody (2079A) [Alexa Fluor® 532] from Novus is a HSP27 antibody to HSP27. This antibody reacts with Human. The HSP27 antibody has been validated for the following applications: Western Blot, Flow
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hsp27 [p ser78] antibody (2079a) [dylight 405]  (Novus Biologicals)
N/A
The HSP27 [p Ser78] Antibody (2079A) [DyLight 405] from Novus is a HSP27 antibody to HSP27. This antibody reacts with Human. The HSP27 antibody has been validated for the following applications: Western Blot, Flow Cytometry,
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hsp27 [p ser78] antibody (2079a) [dylight 680]  (Novus Biologicals)
N/A
The HSP27 [p Ser78] Antibody (2079A) [DyLight 680] from Novus is a HSP27 antibody to HSP27. This antibody reacts with Human. The HSP27 antibody has been validated for the following applications: Western Blot, Flow Cytometry,
   Buy from Supplier
hsp27 [p ser78] antibody (2079a) [alexa fluor® 488]  (Novus Biologicals)
N/A
The HSP27 [p Ser78] Antibody (2079A) [Alexa Fluor® 488] from Novus is a HSP27 antibody to HSP27. This antibody reacts with Human. The HSP27 antibody has been validated for the following applications: Western Blot, Flow
   Buy from Supplier
hsp27 [p ser78] antibody (2079a) [alexa fluor® 647]  (Novus Biologicals)
N/A
The HSP27 [p Ser78] Antibody (2079A) [Alexa Fluor® 647] from Novus is a HSP27 antibody to HSP27. This antibody reacts with Human. The HSP27 antibody has been validated for the following applications: Western Blot, Flow
   Buy from Supplier

Image Search Results


Schematic model representing the regulation of actin stress fibers and focal adhesions by ER. The model shows activation of a signaling cascade that involves ER interaction with α2β1, activation of cAMP, PKA, and FAK, followed by the transient activation of p38 MAPK and Hsp27, and ultimately disassembly of actin stress fibers and focal adhesions. The various blocking agents are also illustrated. For additional details see the text.

Journal: The Journal of Cell Biology

Article Title: Endorepellin causes endothelial cell disassembly of actin cytoskeleton and focal adhesions through α2β1 integrin

doi: 10.1083/jcb.200401150

Figure Lengend Snippet: Schematic model representing the regulation of actin stress fibers and focal adhesions by ER. The model shows activation of a signaling cascade that involves ER interaction with α2β1, activation of cAMP, PKA, and FAK, followed by the transient activation of p38 MAPK and Hsp27, and ultimately disassembly of actin stress fibers and focal adhesions. The various blocking agents are also illustrated. For additional details see the text.

Article Snippet: Antibodies against Erk1/2 (Promega), P-Erk1/2 (Cell Signaling), FAK (BD Biosciences), P-FAK(Y397) (Upstate Biotechnology), p38 and P-p38 (Cell Signaling), total Hsp27 and P-Hsp27 (Santa Cruz Biotechnology, Inc.) were also used in immunoblottings.

Techniques: Activation Assay, Blocking Assay

Heat-shock protein 27 (Hsp27) is associated with LYM resistance to DOX and decreased HLA-DR expression on monocytes. (A) LYM co-cultured with monocytes with and without DOX have increased intracellular Hsp27 expression . Quantitative analysis of LYM (Granta-519) intracellular Hsp27 expression by immunoblot is shown (mean ± SD, n = 3). Representative immunoblot images are shown above each condition. (B) Quantitative analysis of LYM intracellular Hsp27 expression by flow cytometry is shown for OCI-Ly3 ( n = 4) and OCI-Ly10 ( n = 6; mean ± SD). Representative histogram of OCI-Ly3 intracellular Hsp27 expression are shown above the corresponding condition (shaded = isotype control; line = Hsp27). (C) Hsp27 can directly induce decreased HLA-DR expression on monocytes in a dose-dependent manner (left panel, n = 4). LYM cells can secrete Hsp27 . Supernatants from LYM cells and monocyte co-culture with and without DOX have significantly higher soluble Hsp27 compared to media (right panel, white bars, left axis). Culture supernatant from LYM co-culture high in Hsp27, but not media or supernatant from normal B cell co-culture, induced decreased HLA-DR expression on normal CD14 + HLA-DR + monocytes (right panel, black bars, right axis: LYM = Granta-519; n = 6; * p < 0.05 compared to control media; Δ p < 0.05 compared to normal B cell and monocyte co-culture supernatant.) (D) More importantly, Hsp27 is detectable in plasma of patients with lymphoma. Increased plasma level of Hsp27 correlated with increased percentage of CD14 + HLA-DR low/neg monocytes in blood (left panel). Patients who were refractory to DOX treatments had higher plasma Hsp27 levels than those who responded to treatments (right panel).

Journal: Oncoimmunology

Article Title: Immune independent crosstalk between lymphoma and myeloid suppressor CD14 + HLA-DR low/neg monocytes mediates chemotherapy resistance

doi: 10.1080/2162402X.2014.996470

Figure Lengend Snippet: Heat-shock protein 27 (Hsp27) is associated with LYM resistance to DOX and decreased HLA-DR expression on monocytes. (A) LYM co-cultured with monocytes with and without DOX have increased intracellular Hsp27 expression . Quantitative analysis of LYM (Granta-519) intracellular Hsp27 expression by immunoblot is shown (mean ± SD, n = 3). Representative immunoblot images are shown above each condition. (B) Quantitative analysis of LYM intracellular Hsp27 expression by flow cytometry is shown for OCI-Ly3 ( n = 4) and OCI-Ly10 ( n = 6; mean ± SD). Representative histogram of OCI-Ly3 intracellular Hsp27 expression are shown above the corresponding condition (shaded = isotype control; line = Hsp27). (C) Hsp27 can directly induce decreased HLA-DR expression on monocytes in a dose-dependent manner (left panel, n = 4). LYM cells can secrete Hsp27 . Supernatants from LYM cells and monocyte co-culture with and without DOX have significantly higher soluble Hsp27 compared to media (right panel, white bars, left axis). Culture supernatant from LYM co-culture high in Hsp27, but not media or supernatant from normal B cell co-culture, induced decreased HLA-DR expression on normal CD14 + HLA-DR + monocytes (right panel, black bars, right axis: LYM = Granta-519; n = 6; * p < 0.05 compared to control media; Δ p < 0.05 compared to normal B cell and monocyte co-culture supernatant.) (D) More importantly, Hsp27 is detectable in plasma of patients with lymphoma. Increased plasma level of Hsp27 correlated with increased percentage of CD14 + HLA-DR low/neg monocytes in blood (left panel). Patients who were refractory to DOX treatments had higher plasma Hsp27 levels than those who responded to treatments (right panel).

Article Snippet: For culture with recombinant human Hsp27 (R&D Systems) at specified concentration, monocytes were cultured in RPMI-1640 media with 10% fetal bovine serum and M-CSF (10 ng/mL) for 3 d.

Techniques: Expressing, Cell Culture, Western Blot, Flow Cytometry, Control, Co-Culture Assay, Clinical Proteomics