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rabbit anti cd45 polyclonal antibody  (Bioss)


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    Structured Review

    Bioss rabbit anti cd45 polyclonal antibody
    Rabbit Anti Cd45 Polyclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 92/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+cd45+polyclonal+antibody/CD45+Polyclonal+Antibody/pm39733869-127-31-37
    Average 92 stars, based on 20 article reviews
    rabbit anti cd45 polyclonal antibody - by Bioz Stars, 2026-09
    92/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Using paracrine effects of Ad-MSCs on keratinocyte cultivation and fabrication of epidermal sheets for improving clinical applications.
    Article Snippet: Recent advances in wound healing have made cell therapy a potential approach for the treatment of various types of skin defects such as trauma, burns, scars and diabetic leg ulcers.. Cultured keratinocytes have been applied to burn patients since 1981.. Patients with acute and chronic wounds can be treated with autologous/allograft cultured keratinocytes.

    Flow Cytometry:

    Article Title: Insights into the protective capacity of human dental pulp stem cells and its secretome in cisplatin-induced nephrotoxicity: effects on oxidative stress and histological changes.
    Article Snippet: Objectives: Acute renal injury (AKI) is a major limiting factor for cisplatin administration.. Recent evidence suggests the potential contribution of mesenchymal stem cells (MSCs) to rehabilitation from several disorders via both direct and indirect routes.. Thus, the present study aimed, for the first time, to explore and compare the reno-protective potential of human dental pulp-derived stem cells (hDPSCs) vs. hDPSC-conditioned medium (hDPSC-CM) in recovery of impaired kidney tissues in a rat animal model of cisplatin-induced AKI.

    Cytometry:

    Article Title: Insights into the protective capacity of human dental pulp stem cells and its secretome in cisplatin-induced nephrotoxicity: effects on oxidative stress and histological changes.
    Article Snippet: Objectives: Acute renal injury (AKI) is a major limiting factor for cisplatin administration.. Recent evidence suggests the potential contribution of mesenchymal stem cells (MSCs) to rehabilitation from several disorders via both direct and indirect routes.. Thus, the present study aimed, for the first time, to explore and compare the reno-protective potential of human dental pulp-derived stem cells (hDPSCs) vs. hDPSC-conditioned medium (hDPSC-CM) in recovery of impaired kidney tissues in a rat animal model of cisplatin-induced AKI.

    Expressing:

    Article Title: Insights into the protective capacity of human dental pulp stem cells and its secretome in cisplatin-induced nephrotoxicity: effects on oxidative stress and histological changes.
    Article Snippet: Objectives: Acute renal injury (AKI) is a major limiting factor for cisplatin administration.. Recent evidence suggests the potential contribution of mesenchymal stem cells (MSCs) to rehabilitation from several disorders via both direct and indirect routes.. Thus, the present study aimed, for the first time, to explore and compare the reno-protective potential of human dental pulp-derived stem cells (hDPSCs) vs. hDPSC-conditioned medium (hDPSC-CM) in recovery of impaired kidney tissues in a rat animal model of cisplatin-induced AKI.

    FACS:

    Article Title: Effects of Human Adipose-derived Stem Cells and Platelet-Rich Plasma on Healing Response of Canine Alveolar Surgical Bone Defects
    Article Snippet: To confirm of the adipose-derived stem cell nature of isolated cells, collected cells at P3 were exposed to flowcytometric analyses (BD Accuri C6 cytometer) to verify the expression of specific cell surface antigens. .. Our employed antibodies for FACS studies included mouse anti-CD44 polyclonal antibody, rabbit anti-CD34 polyclonal antibody (from antibodies-online, Aachen, Germany), mouse anti- CD90 monoclonal antibody (from Novus Biologicals, Littleton, Colorado, USA), and rabbit anti-CD45 polyclonal antibody (from Bioss Inc., Woburn, MA, USA) ( 5 ). ..



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    Bioss rabbit anti cd45 polyclonal antibody
    Rabbit Anti Cd45 Polyclonal Antibody, supplied by Bioss, 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/rabbit+anti+cd45+polyclonal+antibody/CD45+Polyclonal+Antibody/pm39733869-127-31-37
    Average 92 stars, based on 1 article reviews
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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.
    Anti Cd45 Rabbit Polyclonal Antibody Gb113885, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Novus Biologicals rabbit polyclonal anti cd45
    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.
    Rabbit Polyclonal Anti Cd45, supplied by Novus Biologicals, 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/rabbit+anti+cd45+polyclonal+antibody/CD45+Antibody+(30-F11)+-+BSA+Free/bio_rxiv__2025__06__22__660900-320-25-30
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    Aviva Systems rabbit polyclonal
    Primary CRY1 antisera/antibodies used in this study.
    Rabbit Polyclonal, supplied by Aviva Systems, 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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    Santa Cruz Biotechnology rabbit igg anti human cd45 polyclonal
    Key resources.
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    Bioss rabbit anti cd45 fitc
    Key resources.
    Rabbit Anti Cd45 Fitc, supplied by Bioss, 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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    Aviva Systems rabbit anti ctb polyclonal antibody
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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

    Key resources.

    Journal: Biochimica et biophysica acta. Molecular basis of disease

    Article Title: Integrated multiomic analysis identifies TRIP13 as a mediator of alveolar epithelial type II cell dysfunction in idiopathic pulmonary fibrosis

    doi: 10.1016/j.bbadis.2024.167572

    Figure Lengend Snippet: Key resources.

    Article Snippet: Rabbit IgG anti-human CD45 polyclonal, unconjugated; 1:200 , Santa Cruz Biotech , Cat# sc-25,590 RRID: AB_2174143.

    Techniques: Plasmid Preparation, Magnetic Beads, Recombinant, Blocking Assay, Lysis, Protease Inhibitor, Red Blood Cell Lysis, Software, Microscopy, Fluorescence, Imaging