anti cd62p Search Results


93
Miltenyi Biotec anti mouse cd62p
Anti Mouse Cd62p, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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Bioss p selectin
P Selectin, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+cd62p/pmc07230012-130-31-33?v=Bioss
Average 94 stars, based on 1 article reviews
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Miltenyi Biotec cd62p
Cd62p, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+cd62p/us12496315-1094-5-7?v=Miltenyi+Biotec
Average 94 stars, based on 1 article reviews
cd62p - by Bioz Stars, 2026-08
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Bio-Rad p selectin mouse pab bio rad
P Selectin Mouse Pab Bio Rad, supplied by Bio-Rad, 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/anti+cd62p/pmc09156680__41467_2022_30669_MOESM1_ESM-1-38-41?v=Bio-Rad
Average 93 stars, based on 1 article reviews
p selectin mouse pab bio rad - by Bioz Stars, 2026-08
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93
Boster Bio antid62p p selectin antibody
Fig. 4 – In vivo targeting ability and MRI performance. (A) In vivo biodistribution of MPDA/Gd 3 + /ICG or FMPDA/Gd 3 + /ICG in the tumor-bearing mice model, and the marked red circle indicates the tumor site. Ex vivo images (B) and the corresponding average signal intensity (C) of the tumor tissue and major organs harvested at 24 h post-injection. (D) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and anti-CD41 antibody, respectively. (E) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and <t>P-selectin</t> antibody, respectively. In vivo T1-weighted images (F) and relative T 1 MRI signal intensity (G) of tumors treated before and after treating with MPDA/Gd 3 + /DOX or FMPDA/Gd 3 + /DOX. ( ∗P < 0.05, n = 3).
Antid62p P Selectin Antibody, supplied by Boster Bio, 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/anti+cd62p/pm36600896-59-0-6?v=Boster+Bio
Average 93 stars, based on 1 article reviews
antid62p p selectin antibody - by Bioz Stars, 2026-08
93/100 stars
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92
Bio-Rad mca883f
Fig. 4 – In vivo targeting ability and MRI performance. (A) In vivo biodistribution of MPDA/Gd 3 + /ICG or FMPDA/Gd 3 + /ICG in the tumor-bearing mice model, and the marked red circle indicates the tumor site. Ex vivo images (B) and the corresponding average signal intensity (C) of the tumor tissue and major organs harvested at 24 h post-injection. (D) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and anti-CD41 antibody, respectively. (E) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and <t>P-selectin</t> antibody, respectively. In vivo T1-weighted images (F) and relative T 1 MRI signal intensity (G) of tumors treated before and after treating with MPDA/Gd 3 + /DOX or FMPDA/Gd 3 + /DOX. ( ∗P < 0.05, n = 3).
Mca883f, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+cd62p/pm12618242-78-22-33?v=Bio-Rad
Average 92 stars, based on 1 article reviews
mca883f - by Bioz Stars, 2026-08
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92
Boster Bio rabbit monoclonal anti cd62p
Fig. 4 – In vivo targeting ability and MRI performance. (A) In vivo biodistribution of MPDA/Gd 3 + /ICG or FMPDA/Gd 3 + /ICG in the tumor-bearing mice model, and the marked red circle indicates the tumor site. Ex vivo images (B) and the corresponding average signal intensity (C) of the tumor tissue and major organs harvested at 24 h post-injection. (D) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and anti-CD41 antibody, respectively. (E) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and <t>P-selectin</t> antibody, respectively. In vivo T1-weighted images (F) and relative T 1 MRI signal intensity (G) of tumors treated before and after treating with MPDA/Gd 3 + /DOX or FMPDA/Gd 3 + /DOX. ( ∗P < 0.05, n = 3).
Rabbit Monoclonal Anti Cd62p, supplied by Boster Bio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+cd62p/pm37983208-94-12-17?v=Boster+Bio
Average 92 stars, based on 1 article reviews
rabbit monoclonal anti cd62p - by Bioz Stars, 2026-08
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91
Boster Bio anti cd62p p selectin antibody
In vitro targeting ability and anti-cancer evaluation. (A) CLSM images of thrombin-activated and non-activated platelets treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 30 min. In the case of competitive assay, thrombin-activated platelets were pretreated with <t>Anti-CD62P</t> antibody for 30 min. (B) CLSM images of LM3 cells treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h or 6 h, respectively. In the case of competitive assay, LM3 cells were pretreated with Anti-CD62P antibody for 30 min. (C) CLSM images of LM3 cells after incubating with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h, in the presence of absence of the activated platelets. (D) The cell viability of LM3 cells treated with free DOX, MPDA/Gd 3+ /DOX or FMPDA/Gd 3+ /DOX at different DOX dose for 48 h. (E) The cell viability of LM3 cells treated with different concentrations of FMPDA/Gd 3+ or FMPDA/Gd 3+ /DOX for 12 h, followed by the treatment with or without NIR irradiation (2 W/cm 2 , 5 min) and then incubation for another 2 h. (F) The fluorescent images of survival LM3 cells in different treatment groups (MPDA= 80 µg/ml). (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P <0.0001, n = 5).
Anti Cd62p P Selectin Antibody, supplied by Boster Bio, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+cd62p/pmc09800939-42-0-6?v=Boster+Bio
Average 91 stars, based on 1 article reviews
anti cd62p p selectin antibody - by Bioz Stars, 2026-08
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90
ImmunoReagents inc rat anti-mouse cd62p antibody
In vitro targeting ability and anti-cancer evaluation. (A) CLSM images of thrombin-activated and non-activated platelets treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 30 min. In the case of competitive assay, thrombin-activated platelets were pretreated with <t>Anti-CD62P</t> antibody for 30 min. (B) CLSM images of LM3 cells treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h or 6 h, respectively. In the case of competitive assay, LM3 cells were pretreated with Anti-CD62P antibody for 30 min. (C) CLSM images of LM3 cells after incubating with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h, in the presence of absence of the activated platelets. (D) The cell viability of LM3 cells treated with free DOX, MPDA/Gd 3+ /DOX or FMPDA/Gd 3+ /DOX at different DOX dose for 48 h. (E) The cell viability of LM3 cells treated with different concentrations of FMPDA/Gd 3+ or FMPDA/Gd 3+ /DOX for 12 h, followed by the treatment with or without NIR irradiation (2 W/cm 2 , 5 min) and then incubation for another 2 h. (F) The fluorescent images of survival LM3 cells in different treatment groups (MPDA= 80 µg/ml). (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P <0.0001, n = 5).
Rat Anti Mouse Cd62p Antibody, supplied by ImmunoReagents inc, 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/anti+cd62p/pmc02761686-77-13-27?v=ImmunoReagents+inc
Average 90 stars, based on 1 article reviews
rat anti-mouse cd62p antibody - by Bioz Stars, 2026-08
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90
Immunotec inc fluorescein (fitc)-conjugated anti-cd62p (clone clb-thromb/6) monoclonal antibodies (mab)
In vitro targeting ability and anti-cancer evaluation. (A) CLSM images of thrombin-activated and non-activated platelets treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 30 min. In the case of competitive assay, thrombin-activated platelets were pretreated with <t>Anti-CD62P</t> antibody for 30 min. (B) CLSM images of LM3 cells treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h or 6 h, respectively. In the case of competitive assay, LM3 cells were pretreated with Anti-CD62P antibody for 30 min. (C) CLSM images of LM3 cells after incubating with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h, in the presence of absence of the activated platelets. (D) The cell viability of LM3 cells treated with free DOX, MPDA/Gd 3+ /DOX or FMPDA/Gd 3+ /DOX at different DOX dose for 48 h. (E) The cell viability of LM3 cells treated with different concentrations of FMPDA/Gd 3+ or FMPDA/Gd 3+ /DOX for 12 h, followed by the treatment with or without NIR irradiation (2 W/cm 2 , 5 min) and then incubation for another 2 h. (F) The fluorescent images of survival LM3 cells in different treatment groups (MPDA= 80 µg/ml). (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P <0.0001, n = 5).
Fluorescein (Fitc) Conjugated Anti Cd62p (Clone Clb Thromb/6) Monoclonal Antibodies (Mab), supplied by Immunotec inc, 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/anti+cd62p/pm16923742-54-11-22?v=Immunotec+inc
Average 90 stars, based on 1 article reviews
fluorescein (fitc)-conjugated anti-cd62p (clone clb-thromb/6) monoclonal antibodies (mab) - by Bioz Stars, 2026-08
90/100 stars
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90
Ancell corporation fitc-conjugated murine anti human cd62p antibody
In vitro targeting ability and anti-cancer evaluation. (A) CLSM images of thrombin-activated and non-activated platelets treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 30 min. In the case of competitive assay, thrombin-activated platelets were pretreated with <t>Anti-CD62P</t> antibody for 30 min. (B) CLSM images of LM3 cells treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h or 6 h, respectively. In the case of competitive assay, LM3 cells were pretreated with Anti-CD62P antibody for 30 min. (C) CLSM images of LM3 cells after incubating with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h, in the presence of absence of the activated platelets. (D) The cell viability of LM3 cells treated with free DOX, MPDA/Gd 3+ /DOX or FMPDA/Gd 3+ /DOX at different DOX dose for 48 h. (E) The cell viability of LM3 cells treated with different concentrations of FMPDA/Gd 3+ or FMPDA/Gd 3+ /DOX for 12 h, followed by the treatment with or without NIR irradiation (2 W/cm 2 , 5 min) and then incubation for another 2 h. (F) The fluorescent images of survival LM3 cells in different treatment groups (MPDA= 80 µg/ml). (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P <0.0001, n = 5).
Fitc Conjugated Murine Anti Human Cd62p Antibody, supplied by Ancell corporation, 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/anti+cd62p/10__36959_slash_584_slash_461-83-8-14?v=Ancell+corporation
Average 90 stars, based on 1 article reviews
fitc-conjugated murine anti human cd62p antibody - by Bioz Stars, 2026-08
90/100 stars
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90
Merck KGaA anti-cd62p-fitc antibody
In vitro targeting ability and anti-cancer evaluation. (A) CLSM images of thrombin-activated and non-activated platelets treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 30 min. In the case of competitive assay, thrombin-activated platelets were pretreated with <t>Anti-CD62P</t> antibody for 30 min. (B) CLSM images of LM3 cells treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h or 6 h, respectively. In the case of competitive assay, LM3 cells were pretreated with Anti-CD62P antibody for 30 min. (C) CLSM images of LM3 cells after incubating with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h, in the presence of absence of the activated platelets. (D) The cell viability of LM3 cells treated with free DOX, MPDA/Gd 3+ /DOX or FMPDA/Gd 3+ /DOX at different DOX dose for 48 h. (E) The cell viability of LM3 cells treated with different concentrations of FMPDA/Gd 3+ or FMPDA/Gd 3+ /DOX for 12 h, followed by the treatment with or without NIR irradiation (2 W/cm 2 , 5 min) and then incubation for another 2 h. (F) The fluorescent images of survival LM3 cells in different treatment groups (MPDA= 80 µg/ml). (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P <0.0001, n = 5).
Anti Cd62p Fitc Antibody, supplied by Merck KGaA, 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/anti+cd62p/pm40003888-256-1-12?v=Merck+KGaA
Average 90 stars, based on 1 article reviews
anti-cd62p-fitc antibody - by Bioz Stars, 2026-08
90/100 stars
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Image Search Results


Fig. 4 – In vivo targeting ability and MRI performance. (A) In vivo biodistribution of MPDA/Gd 3 + /ICG or FMPDA/Gd 3 + /ICG in the tumor-bearing mice model, and the marked red circle indicates the tumor site. Ex vivo images (B) and the corresponding average signal intensity (C) of the tumor tissue and major organs harvested at 24 h post-injection. (D) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and anti-CD41 antibody, respectively. (E) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and P-selectin antibody, respectively. In vivo T1-weighted images (F) and relative T 1 MRI signal intensity (G) of tumors treated before and after treating with MPDA/Gd 3 + /DOX or FMPDA/Gd 3 + /DOX. ( ∗P < 0.05, n = 3).

Journal: Asian journal of pharmaceutical sciences

Article Title: Fucoidan-based dual-targeting mesoporous polydopamine for enhanced MRI-guided chemo-photothermal therapy of HCC via P-selectin-mediated drug delivery.

doi: 10.1016/j.ajps.2022.08.004

Figure Lengend Snippet: Fig. 4 – In vivo targeting ability and MRI performance. (A) In vivo biodistribution of MPDA/Gd 3 + /ICG or FMPDA/Gd 3 + /ICG in the tumor-bearing mice model, and the marked red circle indicates the tumor site. Ex vivo images (B) and the corresponding average signal intensity (C) of the tumor tissue and major organs harvested at 24 h post-injection. (D) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and anti-CD41 antibody, respectively. (E) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and P-selectin antibody, respectively. In vivo T1-weighted images (F) and relative T 1 MRI signal intensity (G) of tumors treated before and after treating with MPDA/Gd 3 + /DOX or FMPDA/Gd 3 + /DOX. ( ∗P < 0.05, n = 3).

Article Snippet: AntiD62P (P-selectin) antibody was purchased from Boster Co., td. (Wuhan, China).

Techniques: In Vivo, Ex Vivo, Injection, Staining

Scheme 1 – In this work, FMDA/Gd 3 + /DOX was prepared for enhanced cancer theranostics. Due to the specific binding ability between fucoidan and p-selectin, this novel theranostic agent could effectively accumulate into tumor site by simultaneously targeting to the activated paltelets and tumor cells, thereby resulting in an enhanced MRI-guided chemo-photothermal combination therapy of HCC.

Journal: Asian journal of pharmaceutical sciences

Article Title: Fucoidan-based dual-targeting mesoporous polydopamine for enhanced MRI-guided chemo-photothermal therapy of HCC via P-selectin-mediated drug delivery.

doi: 10.1016/j.ajps.2022.08.004

Figure Lengend Snippet: Scheme 1 – In this work, FMDA/Gd 3 + /DOX was prepared for enhanced cancer theranostics. Due to the specific binding ability between fucoidan and p-selectin, this novel theranostic agent could effectively accumulate into tumor site by simultaneously targeting to the activated paltelets and tumor cells, thereby resulting in an enhanced MRI-guided chemo-photothermal combination therapy of HCC.

Article Snippet: AntiD62P (P-selectin) antibody was purchased from Boster Co., td. (Wuhan, China).

Techniques: Binding Assay

In vitro targeting ability and anti-cancer evaluation. (A) CLSM images of thrombin-activated and non-activated platelets treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 30 min. In the case of competitive assay, thrombin-activated platelets were pretreated with Anti-CD62P antibody for 30 min. (B) CLSM images of LM3 cells treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h or 6 h, respectively. In the case of competitive assay, LM3 cells were pretreated with Anti-CD62P antibody for 30 min. (C) CLSM images of LM3 cells after incubating with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h, in the presence of absence of the activated platelets. (D) The cell viability of LM3 cells treated with free DOX, MPDA/Gd 3+ /DOX or FMPDA/Gd 3+ /DOX at different DOX dose for 48 h. (E) The cell viability of LM3 cells treated with different concentrations of FMPDA/Gd 3+ or FMPDA/Gd 3+ /DOX for 12 h, followed by the treatment with or without NIR irradiation (2 W/cm 2 , 5 min) and then incubation for another 2 h. (F) The fluorescent images of survival LM3 cells in different treatment groups (MPDA= 80 µg/ml). (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P <0.0001, n = 5).

Journal: Asian Journal of Pharmaceutical Sciences

Article Title: Fucoidan-based dual-targeting mesoporous polydopamine for enhanced MRI-guided chemo-photothermal therapy of HCC via P-selectin-mediated drug delivery

doi: 10.1016/j.ajps.2022.08.004

Figure Lengend Snippet: In vitro targeting ability and anti-cancer evaluation. (A) CLSM images of thrombin-activated and non-activated platelets treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 30 min. In the case of competitive assay, thrombin-activated platelets were pretreated with Anti-CD62P antibody for 30 min. (B) CLSM images of LM3 cells treated with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h or 6 h, respectively. In the case of competitive assay, LM3 cells were pretreated with Anti-CD62P antibody for 30 min. (C) CLSM images of LM3 cells after incubating with FMPDA/Gd 3+ /DOX or MPDA/Gd 3+ /DOX for 1 h, in the presence of absence of the activated platelets. (D) The cell viability of LM3 cells treated with free DOX, MPDA/Gd 3+ /DOX or FMPDA/Gd 3+ /DOX at different DOX dose for 48 h. (E) The cell viability of LM3 cells treated with different concentrations of FMPDA/Gd 3+ or FMPDA/Gd 3+ /DOX for 12 h, followed by the treatment with or without NIR irradiation (2 W/cm 2 , 5 min) and then incubation for another 2 h. (F) The fluorescent images of survival LM3 cells in different treatment groups (MPDA= 80 µg/ml). (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P <0.0001, n = 5).

Article Snippet: Anti-CD62P (P-selectin) antibody was purchased from Boster Co., Ltd. (Wuhan, China).

Techniques: In Vitro, Irradiation, Incubation

In vivo targeting ability and MRI performance. (A) In vivo biodistribution of MPDA/Gd 3+ /ICG or FMPDA/Gd 3+ /ICG in the tumor-bearing mice model, and the marked red circle indicates the tumor site. Ex vivo images (B) and the corresponding average signal intensity (C) of the tumor tissue and major organs harvested at 24 h post-injection. (D) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and anti-CD41 antibody, respectively. (E) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and P-selectin antibody, respectively. In vivo T1-weighted images (F) and relative T 1 MRI signal intensity (G) of tumors treated before and after treating with MPDA/Gd 3+ /DOX or FMPDA/Gd 3+ /DOX. (* P < 0.05, n = 3).

Journal: Asian Journal of Pharmaceutical Sciences

Article Title: Fucoidan-based dual-targeting mesoporous polydopamine for enhanced MRI-guided chemo-photothermal therapy of HCC via P-selectin-mediated drug delivery

doi: 10.1016/j.ajps.2022.08.004

Figure Lengend Snippet: In vivo targeting ability and MRI performance. (A) In vivo biodistribution of MPDA/Gd 3+ /ICG or FMPDA/Gd 3+ /ICG in the tumor-bearing mice model, and the marked red circle indicates the tumor site. Ex vivo images (B) and the corresponding average signal intensity (C) of the tumor tissue and major organs harvested at 24 h post-injection. (D) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and anti-CD41 antibody, respectively. (E) Fluorescent images of tumor frozen sections harvested at 24 h post-injection, in which the tumor tissue was stained with DAPI and P-selectin antibody, respectively. In vivo T1-weighted images (F) and relative T 1 MRI signal intensity (G) of tumors treated before and after treating with MPDA/Gd 3+ /DOX or FMPDA/Gd 3+ /DOX. (* P < 0.05, n = 3).

Article Snippet: Anti-CD62P (P-selectin) antibody was purchased from Boster Co., Ltd. (Wuhan, China).

Techniques: In Vivo, Ex Vivo, Injection, Staining

In this work, FMDA/Gd 3+ /DOX was prepared for enhanced cancer theranostics. Due to the specific binding ability between fucoidan and p-selectin, this novel theranostic agent could effectively accumulate into tumor site by simultaneously targeting to the activated paltelets and tumor cells, thereby resulting in an enhanced MRI-guided chemo-photothermal combination therapy of HCC.

Journal: Asian Journal of Pharmaceutical Sciences

Article Title: Fucoidan-based dual-targeting mesoporous polydopamine for enhanced MRI-guided chemo-photothermal therapy of HCC via P-selectin-mediated drug delivery

doi: 10.1016/j.ajps.2022.08.004

Figure Lengend Snippet: In this work, FMDA/Gd 3+ /DOX was prepared for enhanced cancer theranostics. Due to the specific binding ability between fucoidan and p-selectin, this novel theranostic agent could effectively accumulate into tumor site by simultaneously targeting to the activated paltelets and tumor cells, thereby resulting in an enhanced MRI-guided chemo-photothermal combination therapy of HCC.

Article Snippet: Anti-CD62P (P-selectin) antibody was purchased from Boster Co., Ltd. (Wuhan, China).

Techniques: Binding Assay