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rabbit polyclonal antibodies against human vegf  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit polyclonal antibodies against human vegf
    A. Endostar plus NP did not significantly increase the DFS of patients with complete resectable NSCLC ( p = 0.814). B. Endostar plus NP significantly increases the DFS of patients with high expression of <t>VEGF</t> ( p = 0.037).
    Rabbit Polyclonal Antibodies Against Human Vegf, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 207 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+antibodies+against+human+vegf/VEGF-C+Antibody/pmc05668083-96-7-13
    Average 94 stars, based on 207 article reviews
    rabbit polyclonal antibodies against human vegf - by Bioz Stars, 2026-09
    94/100 stars

    Images

    1) Product Images from "Endostar in combination with postoperative adjuvant chemotherapy prolongs the disease free survival of stage IIIA NSCLC patients with high VEGF expression"

    Article Title: Endostar in combination with postoperative adjuvant chemotherapy prolongs the disease free survival of stage IIIA NSCLC patients with high VEGF expression

    Journal: Oncotarget

    doi: 10.18632/oncotarget.19114

    A. Endostar plus NP did not significantly increase the DFS of patients with complete resectable NSCLC ( p = 0.814). B. Endostar plus NP significantly increases the DFS of patients with high expression of VEGF ( p = 0.037).
    Figure Legend Snippet: A. Endostar plus NP did not significantly increase the DFS of patients with complete resectable NSCLC ( p = 0.814). B. Endostar plus NP significantly increases the DFS of patients with high expression of VEGF ( p = 0.037).

    Techniques Used: Expressing

    The DFS and OS of patients with  VEGF  expression status
    Figure Legend Snippet: The DFS and OS of patients with VEGF expression status

    Techniques Used: Expressing

    A. Endostar plus NP prolonged the OS of patients with complete resectable NSCLC but with no statistical significance ( P = 0.962). B. Endostar plus NP did not significantly increase NSCLC patient’s OS regardless expression status of VEGF ( P = 0.182).
    Figure Legend Snippet: A. Endostar plus NP prolonged the OS of patients with complete resectable NSCLC but with no statistical significance ( P = 0.962). B. Endostar plus NP did not significantly increase NSCLC patient’s OS regardless expression status of VEGF ( P = 0.182).

    Techniques Used: Expressing

    Related Articles

    Incubation:

    Article Title: Endostar in combination with postoperative adjuvant chemotherapy prolongs the disease free survival of stage IIIA NSCLC patients with high VEGF expression
    Article Snippet: .. Then the slides were incubated with the rabbit polyclonal antibodies against human VEGF (Cell Signaling Technology, Boston, MA, USA) at 1:50 dilution in PBS at 4 °C overnight. .. The next day after washing with PBS, the sections were incubated with secondary HRP conjugated goat anti-rabbit antibody (Cell Signaling Technology) and hydrogen peroxide for 30 min.



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    Image Search Results


    (A) Gene expression VEGF 165 in HBMSC, HUVEC, co-HBMSC and co-HUVEC after being cultured for different time. Data of gene expression was quantified relative to the same gene expression in HBMSC after 6 hours of culture (same in the following gene expression analysis). a and b indicated the difference p≤0.05 or p≤0.01, respectively. Interestingly, we found that VEGF 165 was only expressed by HBMSC and co-HBMSC and VEGF 165 expression in co-HBMSC is much higher than that in HBMSC during 6 hours–18 hours. However, this upregulation in co-HBMSC diminished at 24 hours. (B) Gene expression of KDR in HBMSC, HUVEC, co-HBMSC and co-HUVEC after being cultured for different time. KDR was mainly expressed by endothelial cells and it was much higher in co-HUVEC than in HUVEC from 14–24 hours. At 6 hours, no significant difference has been observed. (C) Gene expression of uPA in HBMSC, HUVEC, co-HBMSC and co-HUVEC after being cultured for different time. uPA has a similar expression style as to the expression of KDR. (D) Gene expression of uPAR in HBMSC, HUVEC, co-HBMSC and co-HUVEC after being cultured for different time. uPAR expressed by all cells and it is higher expressed by co-cultured cells as compared to mono-cultured cell. (E) Immunofluorescence staining of KDR in cells in green. Nuclear was stained in blue with DAPI. Scare bars represent 50 µm. It can be clearly seen that the expression of KDR is much higher in co-cultured cells than in mono-cultured HUVEC. No much KDR could be detected in HBMSC by immunofluorescence.

    Journal: PLoS ONE

    Article Title: The Role of Vascular Actors in Two Dimensional Dialogue of Human Bone Marrow Stromal Cell and Endothelial Cell for Inducing Self-Assembled Network

    doi: 10.1371/journal.pone.0016767

    Figure Lengend Snippet: (A) Gene expression VEGF 165 in HBMSC, HUVEC, co-HBMSC and co-HUVEC after being cultured for different time. Data of gene expression was quantified relative to the same gene expression in HBMSC after 6 hours of culture (same in the following gene expression analysis). a and b indicated the difference p≤0.05 or p≤0.01, respectively. Interestingly, we found that VEGF 165 was only expressed by HBMSC and co-HBMSC and VEGF 165 expression in co-HBMSC is much higher than that in HBMSC during 6 hours–18 hours. However, this upregulation in co-HBMSC diminished at 24 hours. (B) Gene expression of KDR in HBMSC, HUVEC, co-HBMSC and co-HUVEC after being cultured for different time. KDR was mainly expressed by endothelial cells and it was much higher in co-HUVEC than in HUVEC from 14–24 hours. At 6 hours, no significant difference has been observed. (C) Gene expression of uPA in HBMSC, HUVEC, co-HBMSC and co-HUVEC after being cultured for different time. uPA has a similar expression style as to the expression of KDR. (D) Gene expression of uPAR in HBMSC, HUVEC, co-HBMSC and co-HUVEC after being cultured for different time. uPAR expressed by all cells and it is higher expressed by co-cultured cells as compared to mono-cultured cell. (E) Immunofluorescence staining of KDR in cells in green. Nuclear was stained in blue with DAPI. Scare bars represent 50 µm. It can be clearly seen that the expression of KDR is much higher in co-cultured cells than in mono-cultured HUVEC. No much KDR could be detected in HBMSC by immunofluorescence.

    Article Snippet: Mouse monoclonal antibody against human VE-cad (Hycult Biotechnology) was used at 15 µg/ml, rabbit polyclonal antibody against human VEGF 165 (Millpore) was used at 10 µg/ml and rabbit polyclonal antibody against human uPAR (American Diagostica Inc.) was used at 5 µg/ml.

    Techniques: Expressing, Cell Culture, Immunofluorescence, Staining

    (A) HBMSC and HUVEC were co-cultured with neutralizing antibodies against VE-cad, VEGF 165 and uPAR for 24 hours. We found that the neutralization of VE-cad, VEGF 165 and uPAR suppressed the formation of self-assembled network in co-culture system without impairing the viability of cells. Addition of isotype control mouse antibody or normal IgG rabbit antibody had no effect on self-assembled network formation. Scare bars represent 200 µm. (B) The migration velocity of co-HUVEC were analyzed from the images taken by time-lapse videomicroscopy observing co-cultures with or without neutralizing antibody. Interestingly, co-HUVEC in co-culture incubated with VE-cad neutralizing antibody was still be able to migrate. The migration speed is very close to the co-HUVEC in co-culture without any neutralizing antibody. However, the neutralization of VEGF 165 and uPAR totally blocked the migration of co-HUVEC in co-culture system.

    Journal: PLoS ONE

    Article Title: The Role of Vascular Actors in Two Dimensional Dialogue of Human Bone Marrow Stromal Cell and Endothelial Cell for Inducing Self-Assembled Network

    doi: 10.1371/journal.pone.0016767

    Figure Lengend Snippet: (A) HBMSC and HUVEC were co-cultured with neutralizing antibodies against VE-cad, VEGF 165 and uPAR for 24 hours. We found that the neutralization of VE-cad, VEGF 165 and uPAR suppressed the formation of self-assembled network in co-culture system without impairing the viability of cells. Addition of isotype control mouse antibody or normal IgG rabbit antibody had no effect on self-assembled network formation. Scare bars represent 200 µm. (B) The migration velocity of co-HUVEC were analyzed from the images taken by time-lapse videomicroscopy observing co-cultures with or without neutralizing antibody. Interestingly, co-HUVEC in co-culture incubated with VE-cad neutralizing antibody was still be able to migrate. The migration speed is very close to the co-HUVEC in co-culture without any neutralizing antibody. However, the neutralization of VEGF 165 and uPAR totally blocked the migration of co-HUVEC in co-culture system.

    Article Snippet: Mouse monoclonal antibody against human VE-cad (Hycult Biotechnology) was used at 15 µg/ml, rabbit polyclonal antibody against human VEGF 165 (Millpore) was used at 10 µg/ml and rabbit polyclonal antibody against human uPAR (American Diagostica Inc.) was used at 5 µg/ml.

    Techniques: Cell Culture, Neutralization, Co-Culture Assay, Migration, Incubation

    (A) Gene expressions of VEGF 165 in HBMSC, HUVEC, Co-HBMSC and co-HUVEC cultured with (bars with shadow) or without VE-cad neutralizing antibody. Neutralization of VE-cad has no strong effects on expression of VEGF 165 . (B) Gene expressions of uPA in HBMSC, HUVEC, Co-HBMSC and co-HUVEC cultured with (bars with shadow) or without VE-cad neutralizing antibody. Neutralization of VE-cad significantly downregulated the expression of uPA in co-HUVEC at 14 hours and 16 hours and this effect decreased at 24 hours. However, the expression of uPA in co-HUVEC still maintained a high level. (C) Gene expressions of uPAR in HBMSC, HUVEC, Co-HBMSC and co-HUVEC cultured with (bars with shadow) or without VE-cad neutralizing antibody. uPAR was transiently affected by neutralization of VE-cad. Its expression statistically decreased in co-HBMSC at 6 hours and 14 hours. (D) Gene expression of uPA in HBMSC, HUVEC, Co-HBMSC and co-HUVEC with (bars with shadow) or without VEGF 165 neutralizing antibody. Neutralization of VEGF 165 strongly suppressed the expression of uPA in co-HUVEC. (E) Gene expression of uPAR in HBMSC, HUVEC, Co-HBMSC and co-HUVEC with (bars with shadow) or without VEGF 165 neutralizing antibody. Gene expression of uPAR in co-cultured cells was downregulated all the time after the addition of VEGF 165 neutralizing antibody. a and b indicated the difference p≤0.05 or p≤0.01, respectively.

    Journal: PLoS ONE

    Article Title: The Role of Vascular Actors in Two Dimensional Dialogue of Human Bone Marrow Stromal Cell and Endothelial Cell for Inducing Self-Assembled Network

    doi: 10.1371/journal.pone.0016767

    Figure Lengend Snippet: (A) Gene expressions of VEGF 165 in HBMSC, HUVEC, Co-HBMSC and co-HUVEC cultured with (bars with shadow) or without VE-cad neutralizing antibody. Neutralization of VE-cad has no strong effects on expression of VEGF 165 . (B) Gene expressions of uPA in HBMSC, HUVEC, Co-HBMSC and co-HUVEC cultured with (bars with shadow) or without VE-cad neutralizing antibody. Neutralization of VE-cad significantly downregulated the expression of uPA in co-HUVEC at 14 hours and 16 hours and this effect decreased at 24 hours. However, the expression of uPA in co-HUVEC still maintained a high level. (C) Gene expressions of uPAR in HBMSC, HUVEC, Co-HBMSC and co-HUVEC cultured with (bars with shadow) or without VE-cad neutralizing antibody. uPAR was transiently affected by neutralization of VE-cad. Its expression statistically decreased in co-HBMSC at 6 hours and 14 hours. (D) Gene expression of uPA in HBMSC, HUVEC, Co-HBMSC and co-HUVEC with (bars with shadow) or without VEGF 165 neutralizing antibody. Neutralization of VEGF 165 strongly suppressed the expression of uPA in co-HUVEC. (E) Gene expression of uPAR in HBMSC, HUVEC, Co-HBMSC and co-HUVEC with (bars with shadow) or without VEGF 165 neutralizing antibody. Gene expression of uPAR in co-cultured cells was downregulated all the time after the addition of VEGF 165 neutralizing antibody. a and b indicated the difference p≤0.05 or p≤0.01, respectively.

    Article Snippet: Mouse monoclonal antibody against human VE-cad (Hycult Biotechnology) was used at 15 µg/ml, rabbit polyclonal antibody against human VEGF 165 (Millpore) was used at 10 µg/ml and rabbit polyclonal antibody against human uPAR (American Diagostica Inc.) was used at 5 µg/ml.

    Techniques: Cell Culture, Neutralization, Expressing

    Primer sequences used in Q-PCR.

    Journal: PLoS ONE

    Article Title: The Role of Vascular Actors in Two Dimensional Dialogue of Human Bone Marrow Stromal Cell and Endothelial Cell for Inducing Self-Assembled Network

    doi: 10.1371/journal.pone.0016767

    Figure Lengend Snippet: Primer sequences used in Q-PCR.

    Article Snippet: Mouse monoclonal antibody against human VE-cad (Hycult Biotechnology) was used at 15 µg/ml, rabbit polyclonal antibody against human VEGF 165 (Millpore) was used at 10 µg/ml and rabbit polyclonal antibody against human uPAR (American Diagostica Inc.) was used at 5 µg/ml.

    Techniques:

    Description and characteristics of the primary antibodies.

    Journal: Biology

    Article Title: Singer’s Nodules: Investigating the Etiopathogenetic Markers Progressing Their Pathogenesis and Clinical Manifestations

    doi: 10.3390/biology10121268

    Figure Lengend Snippet: Description and characteristics of the primary antibodies.

    Article Snippet: VEGF , Polyclonal rabbit AB against human AG , - , 1:100 , orb191500 , Biorbyt (UK).

    Techniques:

    A. Endostar plus NP did not significantly increase the DFS of patients with complete resectable NSCLC ( p = 0.814). B. Endostar plus NP significantly increases the DFS of patients with high expression of VEGF ( p = 0.037).

    Journal: Oncotarget

    Article Title: Endostar in combination with postoperative adjuvant chemotherapy prolongs the disease free survival of stage IIIA NSCLC patients with high VEGF expression

    doi: 10.18632/oncotarget.19114

    Figure Lengend Snippet: A. Endostar plus NP did not significantly increase the DFS of patients with complete resectable NSCLC ( p = 0.814). B. Endostar plus NP significantly increases the DFS of patients with high expression of VEGF ( p = 0.037).

    Article Snippet: Then the slides were incubated with the rabbit polyclonal antibodies against human VEGF (Cell Signaling Technology, Boston, MA, USA) at 1:50 dilution in PBS at 4 °C overnight.

    Techniques: Expressing

    The DFS and OS of patients with  VEGF  expression status

    Journal: Oncotarget

    Article Title: Endostar in combination with postoperative adjuvant chemotherapy prolongs the disease free survival of stage IIIA NSCLC patients with high VEGF expression

    doi: 10.18632/oncotarget.19114

    Figure Lengend Snippet: The DFS and OS of patients with VEGF expression status

    Article Snippet: Then the slides were incubated with the rabbit polyclonal antibodies against human VEGF (Cell Signaling Technology, Boston, MA, USA) at 1:50 dilution in PBS at 4 °C overnight.

    Techniques: Expressing

    A. Endostar plus NP prolonged the OS of patients with complete resectable NSCLC but with no statistical significance ( P = 0.962). B. Endostar plus NP did not significantly increase NSCLC patient’s OS regardless expression status of VEGF ( P = 0.182).

    Journal: Oncotarget

    Article Title: Endostar in combination with postoperative adjuvant chemotherapy prolongs the disease free survival of stage IIIA NSCLC patients with high VEGF expression

    doi: 10.18632/oncotarget.19114

    Figure Lengend Snippet: A. Endostar plus NP prolonged the OS of patients with complete resectable NSCLC but with no statistical significance ( P = 0.962). B. Endostar plus NP did not significantly increase NSCLC patient’s OS regardless expression status of VEGF ( P = 0.182).

    Article Snippet: Then the slides were incubated with the rabbit polyclonal antibodies against human VEGF (Cell Signaling Technology, Boston, MA, USA) at 1:50 dilution in PBS at 4 °C overnight.

    Techniques: Expressing