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cd45 rabbit polyclonal antibody  (Proteintech)


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    Structured Review

    Proteintech cd45 rabbit polyclonal antibody
    Cd45 Rabbit Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 231 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cd45+rabbit+polyclonal+antibody/10__3892_slash_wasj__2025__387-61-95-103?v=Proteintech
    Average 96 stars, based on 231 article reviews
    cd45 rabbit polyclonal antibody - by Bioz Stars, 2026-08
    96/100 stars

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    Servicebio Inc anti-cd45 rabbit polyclonal antibody gb113885
    a In vivo fluorescence imaging of tumor-bearing mice 24 h after intravenous injection of M Cy5.5 As and M Cy5.5 AHAs ( n = 3 mice). The unit of the scale bar is ×10 9 [p/s/cm 2 /sr]/[µW/cm 2 ]. b Left: Confocal fluorescence imaging of tumor sections after administration of M Cy5.5 As and M Cy5.5 AHAs. The 4T1 tumor cells and immune cells were indicated as CD44 and <t>CD45</t> <t>positive</t> cells (red fluorescence), respectively. M Cy5.5 As and M Cy5.5 AHAs were pseudo-colored with green fluorescence. DAPI (blue fluorescence) was used to label the nuclei. Scale bars: 15 µm. Right: Values of Pearson’s correlation coefficient between Cy5.5-incorporated NPs and 4T1 tumor cells or immune cells. Data are represented as mean ± SD ( n = 10 independent samples). P values were calculated using an unpaired two-tailed Student’s t test. c Average tumor growth curves. Data are represented as mean ± SD ( n = 6 mice). P values were calculated using a two-way ANOVA followed by Tukey’s multiple comparisons test. d Survival curves of the mice receiving indicated treatment ( n = 6 mice). P values were calculated using a log-rank (Mantel–Cox) test. e The Asn levels in tumor cells isolated from tumors on day 26 after indicated treatment. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. f Heatmap of mRNA levels of ASNS , PSAT1 , GPT2 , MTHFD2 , and SLC1A5 in tumor cells isolated from tumors after indicated treatment. g Left: representative H&E-stained sections of lungs from indicated groups. Metastatic tumors are indicated with black dotted circles. Scale bars: 100 μm. See also Supplementary Fig. for complete data. Right: the number of tumor foci in lungs after indicated treatment. Data are represented as mean ± SD ( n = 3 mice). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. h , i Expression levels of N-cadherin ( h ) and E-cadherin ( i ) in tumors after indicated treatments. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. Asn asparagine, Cy5.5 cyanine 5.5, Rot rotenone, ASNase L -asparaginase. Source data are provided as a Source Data file.
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    a In vivo fluorescence imaging of tumor-bearing mice 24 h after intravenous injection of M Cy5.5 As and M Cy5.5 AHAs ( n = 3 mice). The unit of the scale bar is ×10 9 [p/s/cm 2 /sr]/[µW/cm 2 ]. b Left: Confocal fluorescence imaging of tumor sections after administration of M Cy5.5 As and M Cy5.5 AHAs. The 4T1 tumor cells and immune cells were indicated as CD44 and <t>CD45</t> <t>positive</t> cells (red fluorescence), respectively. M Cy5.5 As and M Cy5.5 AHAs were pseudo-colored with green fluorescence. DAPI (blue fluorescence) was used to label the nuclei. Scale bars: 15 µm. Right: Values of Pearson’s correlation coefficient between Cy5.5-incorporated NPs and 4T1 tumor cells or immune cells. Data are represented as mean ± SD ( n = 10 independent samples). P values were calculated using an unpaired two-tailed Student’s t test. c Average tumor growth curves. Data are represented as mean ± SD ( n = 6 mice). P values were calculated using a two-way ANOVA followed by Tukey’s multiple comparisons test. d Survival curves of the mice receiving indicated treatment ( n = 6 mice). P values were calculated using a log-rank (Mantel–Cox) test. e The Asn levels in tumor cells isolated from tumors on day 26 after indicated treatment. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. f Heatmap of mRNA levels of ASNS , PSAT1 , GPT2 , MTHFD2 , and SLC1A5 in tumor cells isolated from tumors after indicated treatment. g Left: representative H&E-stained sections of lungs from indicated groups. Metastatic tumors are indicated with black dotted circles. Scale bars: 100 μm. See also Supplementary Fig. for complete data. Right: the number of tumor foci in lungs after indicated treatment. Data are represented as mean ± SD ( n = 3 mice). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. h , i Expression levels of N-cadherin ( h ) and E-cadherin ( i ) in tumors after indicated treatments. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. Asn asparagine, Cy5.5 cyanine 5.5, Rot rotenone, ASNase L -asparaginase. Source data are provided as a Source Data file.
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    Image Search Results


    a In vivo fluorescence imaging of tumor-bearing mice 24 h after intravenous injection of M Cy5.5 As and M Cy5.5 AHAs ( n = 3 mice). The unit of the scale bar is ×10 9 [p/s/cm 2 /sr]/[µW/cm 2 ]. b Left: Confocal fluorescence imaging of tumor sections after administration of M Cy5.5 As and M Cy5.5 AHAs. The 4T1 tumor cells and immune cells were indicated as CD44 and CD45 positive cells (red fluorescence), respectively. M Cy5.5 As and M Cy5.5 AHAs were pseudo-colored with green fluorescence. DAPI (blue fluorescence) was used to label the nuclei. Scale bars: 15 µm. Right: Values of Pearson’s correlation coefficient between Cy5.5-incorporated NPs and 4T1 tumor cells or immune cells. Data are represented as mean ± SD ( n = 10 independent samples). P values were calculated using an unpaired two-tailed Student’s t test. c Average tumor growth curves. Data are represented as mean ± SD ( n = 6 mice). P values were calculated using a two-way ANOVA followed by Tukey’s multiple comparisons test. d Survival curves of the mice receiving indicated treatment ( n = 6 mice). P values were calculated using a log-rank (Mantel–Cox) test. e The Asn levels in tumor cells isolated from tumors on day 26 after indicated treatment. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. f Heatmap of mRNA levels of ASNS , PSAT1 , GPT2 , MTHFD2 , and SLC1A5 in tumor cells isolated from tumors after indicated treatment. g Left: representative H&E-stained sections of lungs from indicated groups. Metastatic tumors are indicated with black dotted circles. Scale bars: 100 μm. See also Supplementary Fig. for complete data. Right: the number of tumor foci in lungs after indicated treatment. Data are represented as mean ± SD ( n = 3 mice). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. h , i Expression levels of N-cadherin ( h ) and E-cadherin ( i ) in tumors after indicated treatments. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. Asn asparagine, Cy5.5 cyanine 5.5, Rot rotenone, ASNase L -asparaginase. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Dual asparagine-depriving nanoparticles against solid tumors

    doi: 10.1038/s41467-025-60798-y

    Figure Lengend Snippet: a In vivo fluorescence imaging of tumor-bearing mice 24 h after intravenous injection of M Cy5.5 As and M Cy5.5 AHAs ( n = 3 mice). The unit of the scale bar is ×10 9 [p/s/cm 2 /sr]/[µW/cm 2 ]. b Left: Confocal fluorescence imaging of tumor sections after administration of M Cy5.5 As and M Cy5.5 AHAs. The 4T1 tumor cells and immune cells were indicated as CD44 and CD45 positive cells (red fluorescence), respectively. M Cy5.5 As and M Cy5.5 AHAs were pseudo-colored with green fluorescence. DAPI (blue fluorescence) was used to label the nuclei. Scale bars: 15 µm. Right: Values of Pearson’s correlation coefficient between Cy5.5-incorporated NPs and 4T1 tumor cells or immune cells. Data are represented as mean ± SD ( n = 10 independent samples). P values were calculated using an unpaired two-tailed Student’s t test. c Average tumor growth curves. Data are represented as mean ± SD ( n = 6 mice). P values were calculated using a two-way ANOVA followed by Tukey’s multiple comparisons test. d Survival curves of the mice receiving indicated treatment ( n = 6 mice). P values were calculated using a log-rank (Mantel–Cox) test. e The Asn levels in tumor cells isolated from tumors on day 26 after indicated treatment. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. f Heatmap of mRNA levels of ASNS , PSAT1 , GPT2 , MTHFD2 , and SLC1A5 in tumor cells isolated from tumors after indicated treatment. g Left: representative H&E-stained sections of lungs from indicated groups. Metastatic tumors are indicated with black dotted circles. Scale bars: 100 μm. See also Supplementary Fig. for complete data. Right: the number of tumor foci in lungs after indicated treatment. Data are represented as mean ± SD ( n = 3 mice). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. h , i Expression levels of N-cadherin ( h ) and E-cadherin ( i ) in tumors after indicated treatments. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using a one-way ANOVA followed by Tukey’s post-hoc test. Asn asparagine, Cy5.5 cyanine 5.5, Rot rotenone, ASNase L -asparaginase. Source data are provided as a Source Data file.

    Article Snippet: Tumor sections were stained with either anti-CD44 rabbit polyclonal antibody (Servicebio, GB112054 ) or anti-CD45 rabbit polyclonal antibody (Servicebio, GB113885 ), and visualized using CLSM.

    Techniques: In Vivo, Fluorescence, Imaging, Injection, Two Tailed Test, Isolation, Staining, Expressing

    a Schematic illustration of the experiment design for post-surgical therapy. Fourteen days after tumor inoculation, primary tumors were removed. Two days later, mice were subjected to various treatments every 3 days for a total of eight doses. On day 75, mice with no sign of tumor relapse and metastasis were challenged with 4T1-Luc cells. b In vivo bioluminescence imaging of the mice after indicated treatment ( n = 6 mice). The unit of the scale bar is ×10 7 p/s/cm 2 /sr. c Tumor growth curves of individual mice after indicated treatment ( n = 6 mice). d Ex vivo bioluminescence images of major organs ( n = 3 mice). The unit of the scale bar is ×10 6 p/s/cm 2 /sr. e Survival curves of the mice receiving the indicated treatment ( n = 6 mice). P values were calculated using a log-rank (Mantel–Cox) test. f In vivo bioluminescence imaging of mice before (day 74) and after (day 75, day 95, and day 105) tumor rechallenge ( n = 5 mice). The unit of the scale bar is ×10 7 p/s/cm 2 /sr. g , h FACS analysis of CD4 + Tcm (gated on CD45 + CD4 + population) ( g ) and CD8 + Tcm cells (gated on CD45 + CD8 + population) ( h ) in splenocytes. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using an unpaired two-tailed Student’s t test. Rot rotenone, ASNase L -asparaginase, He heart, Li liver, Sp spleen, Lu lung, Ki kidney, Tcm central memory T. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Dual asparagine-depriving nanoparticles against solid tumors

    doi: 10.1038/s41467-025-60798-y

    Figure Lengend Snippet: a Schematic illustration of the experiment design for post-surgical therapy. Fourteen days after tumor inoculation, primary tumors were removed. Two days later, mice were subjected to various treatments every 3 days for a total of eight doses. On day 75, mice with no sign of tumor relapse and metastasis were challenged with 4T1-Luc cells. b In vivo bioluminescence imaging of the mice after indicated treatment ( n = 6 mice). The unit of the scale bar is ×10 7 p/s/cm 2 /sr. c Tumor growth curves of individual mice after indicated treatment ( n = 6 mice). d Ex vivo bioluminescence images of major organs ( n = 3 mice). The unit of the scale bar is ×10 6 p/s/cm 2 /sr. e Survival curves of the mice receiving the indicated treatment ( n = 6 mice). P values were calculated using a log-rank (Mantel–Cox) test. f In vivo bioluminescence imaging of mice before (day 74) and after (day 75, day 95, and day 105) tumor rechallenge ( n = 5 mice). The unit of the scale bar is ×10 7 p/s/cm 2 /sr. g , h FACS analysis of CD4 + Tcm (gated on CD45 + CD4 + population) ( g ) and CD8 + Tcm cells (gated on CD45 + CD8 + population) ( h ) in splenocytes. Data are represented as mean ± SD ( n = 3 independent samples). P values were calculated using an unpaired two-tailed Student’s t test. Rot rotenone, ASNase L -asparaginase, He heart, Li liver, Sp spleen, Lu lung, Ki kidney, Tcm central memory T. Source data are provided as a Source Data file.

    Article Snippet: Tumor sections were stained with either anti-CD44 rabbit polyclonal antibody (Servicebio, GB112054 ) or anti-CD45 rabbit polyclonal antibody (Servicebio, GB113885 ), and visualized using CLSM.

    Techniques: In Vivo, Imaging, Ex Vivo, Two Tailed Test

    Primary CRY1 antisera/antibodies used in this study.

    Journal: The FASEB Journal

    Article Title: Full‐Length Cryptochrome 1 in the Outer Segments of the Retinal Blue Cone Photoreceptors in Humans and Great Apes Suggests a Role Beyond Transcriptional Repression

    doi: 10.1096/fj.202402614R

    Figure Lengend Snippet: Primary CRY1 antisera/antibodies used in this study.

    Article Snippet: rb‐α‐CRY1 ARP59758_P050 , Rabbit polyclonal , hCRY1 sequence 151–200 , IHC: 1:200 , Aviva Systems Biology, San Diego, CA, USA.

    Techniques: Sequencing