bpf Search Results


93
Mini-Circuits mini circuits bpf a60
Mini Circuits Bpf A60, supplied by Mini-Circuits, 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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Thorlabs 3.3 thz bpf
3.3 Thz Bpf, supplied by Thorlabs, 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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Accustandard Inc 4,4’- methylenediphenol (bpf)
4,4’ Methylenediphenol (Bpf), supplied by Accustandard 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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OptiGrate Corp optical bragg grating bpf-800
Optical Bragg Grating Bpf 800, supplied by OptiGrate Corp, 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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Average 90 stars, based on 1 article reviews
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Haemonetics bpf high efficiency leukocyte reduction filtration system
A, Flow cytometric plots display intracellular staining (ICS) of apheresis mononuclear cells (MNC) derived from an apheresis procedure where the Optia was primed with ABO-matched whole blood from a heterologous donor (no leukoreduction). Cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets. B, Flow cytometric plots display surface CD45 staining of blood pre- (left) and post-leukoreduction (right) with Haemonetics <t>BPF</t> High Efficiency Leukocyte Reduction Filtration System. Plots are gated on live cells. Gates denote granulocyte (“Gran”) and lymphocyte (“Lymph”) frequencies. Box at the top of each plot shows white blood cell count (WBC, x103 per μL) and red blood cell count (RBC, x106 per μL) in each sample, as measured by complete blood count. C, Flow cytometric plots display ICS of apheresis MNC derived from an apheresis procedure where the Optia was primed <t>with</t> <t>leukoreduced,</t> ABO-matched whole blood from a heterologous donor (top) or ICS of peripheral blood mononuclear cells (PBMC) isolated from a blood draw taken prior to leukapheresis (bottom). As in panel A, cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets.
Bpf High Efficiency Leukocyte Reduction Filtration System, supplied by Haemonetics, 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/result/bpf high efficiency leukocyte reduction filtration system/product/Haemonetics
Average 90 stars, based on 1 article reviews
bpf high efficiency leukocyte reduction filtration system - by Bioz Stars, 2026-03
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Thorlabs 930-nm bpf thorlabs fb930-10
A, Flow cytometric plots display intracellular staining (ICS) of apheresis mononuclear cells (MNC) derived from an apheresis procedure where the Optia was primed with ABO-matched whole blood from a heterologous donor (no leukoreduction). Cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets. B, Flow cytometric plots display surface CD45 staining of blood pre- (left) and post-leukoreduction (right) with Haemonetics <t>BPF</t> High Efficiency Leukocyte Reduction Filtration System. Plots are gated on live cells. Gates denote granulocyte (“Gran”) and lymphocyte (“Lymph”) frequencies. Box at the top of each plot shows white blood cell count (WBC, x103 per μL) and red blood cell count (RBC, x106 per μL) in each sample, as measured by complete blood count. C, Flow cytometric plots display ICS of apheresis MNC derived from an apheresis procedure where the Optia was primed <t>with</t> <t>leukoreduced,</t> ABO-matched whole blood from a heterologous donor (top) or ICS of peripheral blood mononuclear cells (PBMC) isolated from a blood draw taken prior to leukapheresis (bottom). As in panel A, cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets.
930 Nm Bpf Thorlabs Fb930 10, supplied by Thorlabs, 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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Average 90 stars, based on 1 article reviews
930-nm bpf thorlabs fb930-10 - by Bioz Stars, 2026-03
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Macklin Inc bpf
A, Flow cytometric plots display intracellular staining (ICS) of apheresis mononuclear cells (MNC) derived from an apheresis procedure where the Optia was primed with ABO-matched whole blood from a heterologous donor (no leukoreduction). Cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets. B, Flow cytometric plots display surface CD45 staining of blood pre- (left) and post-leukoreduction (right) with Haemonetics <t>BPF</t> High Efficiency Leukocyte Reduction Filtration System. Plots are gated on live cells. Gates denote granulocyte (“Gran”) and lymphocyte (“Lymph”) frequencies. Box at the top of each plot shows white blood cell count (WBC, x103 per μL) and red blood cell count (RBC, x106 per μL) in each sample, as measured by complete blood count. C, Flow cytometric plots display ICS of apheresis MNC derived from an apheresis procedure where the Optia was primed <t>with</t> <t>leukoreduced,</t> ABO-matched whole blood from a heterologous donor (top) or ICS of peripheral blood mononuclear cells (PBMC) isolated from a blood draw taken prior to leukapheresis (bottom). As in panel A, cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets.
Bpf, supplied by Macklin 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/result/bpf/product/Macklin Inc
Average 90 stars, based on 1 article reviews
bpf - by Bioz Stars, 2026-03
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90
Accustandard Inc bpf
A, Flow cytometric plots display intracellular staining (ICS) of apheresis mononuclear cells (MNC) derived from an apheresis procedure where the Optia was primed with ABO-matched whole blood from a heterologous donor (no leukoreduction). Cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets. B, Flow cytometric plots display surface CD45 staining of blood pre- (left) and post-leukoreduction (right) with Haemonetics <t>BPF</t> High Efficiency Leukocyte Reduction Filtration System. Plots are gated on live cells. Gates denote granulocyte (“Gran”) and lymphocyte (“Lymph”) frequencies. Box at the top of each plot shows white blood cell count (WBC, x103 per μL) and red blood cell count (RBC, x106 per μL) in each sample, as measured by complete blood count. C, Flow cytometric plots display ICS of apheresis MNC derived from an apheresis procedure where the Optia was primed <t>with</t> <t>leukoreduced,</t> ABO-matched whole blood from a heterologous donor (top) or ICS of peripheral blood mononuclear cells (PBMC) isolated from a blood draw taken prior to leukapheresis (bottom). As in panel A, cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets.
Bpf, supplied by Accustandard 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/result/bpf/product/Accustandard Inc
Average 90 stars, based on 1 article reviews
bpf - by Bioz Stars, 2026-03
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90
Thorlabs bpf and a rotation stage ell18k/m
A, Flow cytometric plots display intracellular staining (ICS) of apheresis mononuclear cells (MNC) derived from an apheresis procedure where the Optia was primed with ABO-matched whole blood from a heterologous donor (no leukoreduction). Cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets. B, Flow cytometric plots display surface CD45 staining of blood pre- (left) and post-leukoreduction (right) with Haemonetics <t>BPF</t> High Efficiency Leukocyte Reduction Filtration System. Plots are gated on live cells. Gates denote granulocyte (“Gran”) and lymphocyte (“Lymph”) frequencies. Box at the top of each plot shows white blood cell count (WBC, x103 per μL) and red blood cell count (RBC, x106 per μL) in each sample, as measured by complete blood count. C, Flow cytometric plots display ICS of apheresis MNC derived from an apheresis procedure where the Optia was primed <t>with</t> <t>leukoreduced,</t> ABO-matched whole blood from a heterologous donor (top) or ICS of peripheral blood mononuclear cells (PBMC) isolated from a blood draw taken prior to leukapheresis (bottom). As in panel A, cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets.
Bpf And A Rotation Stage Ell18k/M, supplied by Thorlabs, 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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Average 90 stars, based on 1 article reviews
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Tokyo Chemical Industry bpf
Mass spectra of metabolites formed during degradation of <t>BPF</t> by strain FM-2. (A) Metabolite I identified as bis(4-hydroxyphenyl)-methanol with trimethylsilylation. (B) Metabolite II identified <t>as</t> <t>DHBP</t> with trimethylsilylation. (C) Metabolite III identified as 1,4-hydroquinone with trimethylsilylation. (D) Metabolite IV identified as 1,4-benzoquinone. (E) Metabolite V identified as 4HB with trimethylsilylation. (F) Metabolite VI tentatively identified as 4-hydroxyphenyl 4-hydroxybenzoate with trimethylsilylation.
Bpf, supplied by Tokyo Chemical Industry, 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/result/bpf/product/Tokyo Chemical Industry
Average 90 stars, based on 1 article reviews
bpf - by Bioz Stars, 2026-03
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Tokyo Chemical Industry edc-contaminated wastewater 107 bpf
Mass spectra of metabolites formed during degradation of <t>BPF</t> by strain FM-2. (A) Metabolite I identified as bis(4-hydroxyphenyl)-methanol with trimethylsilylation. (B) Metabolite II identified <t>as</t> <t>DHBP</t> with trimethylsilylation. (C) Metabolite III identified as 1,4-hydroquinone with trimethylsilylation. (D) Metabolite IV identified as 1,4-benzoquinone. (E) Metabolite V identified as 4HB with trimethylsilylation. (F) Metabolite VI tentatively identified as 4-hydroxyphenyl 4-hydroxybenzoate with trimethylsilylation.
Edc Contaminated Wastewater 107 Bpf, supplied by Tokyo Chemical Industry, 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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Average 90 stars, based on 1 article reviews
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Cambridge Isotope Laboratories bpf bpf13 c12
Mass spectra of metabolites formed during degradation of <t>BPF</t> by strain FM-2. (A) Metabolite I identified as bis(4-hydroxyphenyl)-methanol with trimethylsilylation. (B) Metabolite II identified <t>as</t> <t>DHBP</t> with trimethylsilylation. (C) Metabolite III identified as 1,4-hydroquinone with trimethylsilylation. (D) Metabolite IV identified as 1,4-benzoquinone. (E) Metabolite V identified as 4HB with trimethylsilylation. (F) Metabolite VI tentatively identified as 4-hydroxyphenyl 4-hydroxybenzoate with trimethylsilylation.
Bpf Bpf13 C12, supplied by Cambridge Isotope Laboratories, 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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Average 90 stars, based on 1 article reviews
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Image Search Results


A, Flow cytometric plots display intracellular staining (ICS) of apheresis mononuclear cells (MNC) derived from an apheresis procedure where the Optia was primed with ABO-matched whole blood from a heterologous donor (no leukoreduction). Cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets. B, Flow cytometric plots display surface CD45 staining of blood pre- (left) and post-leukoreduction (right) with Haemonetics BPF High Efficiency Leukocyte Reduction Filtration System. Plots are gated on live cells. Gates denote granulocyte (“Gran”) and lymphocyte (“Lymph”) frequencies. Box at the top of each plot shows white blood cell count (WBC, x103 per μL) and red blood cell count (RBC, x106 per μL) in each sample, as measured by complete blood count. C, Flow cytometric plots display ICS of apheresis MNC derived from an apheresis procedure where the Optia was primed with leukoreduced, ABO-matched whole blood from a heterologous donor (top) or ICS of peripheral blood mononuclear cells (PBMC) isolated from a blood draw taken prior to leukapheresis (bottom). As in panel A, cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets.

Journal: Journal of clinical apheresis

Article Title: Terumo Spectra Optia leukapheresis of cynomolgus macaques for hematopoietic stem cell and T cell collection

doi: 10.1002/jca.21842

Figure Lengend Snippet: A, Flow cytometric plots display intracellular staining (ICS) of apheresis mononuclear cells (MNC) derived from an apheresis procedure where the Optia was primed with ABO-matched whole blood from a heterologous donor (no leukoreduction). Cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets. B, Flow cytometric plots display surface CD45 staining of blood pre- (left) and post-leukoreduction (right) with Haemonetics BPF High Efficiency Leukocyte Reduction Filtration System. Plots are gated on live cells. Gates denote granulocyte (“Gran”) and lymphocyte (“Lymph”) frequencies. Box at the top of each plot shows white blood cell count (WBC, x103 per μL) and red blood cell count (RBC, x106 per μL) in each sample, as measured by complete blood count. C, Flow cytometric plots display ICS of apheresis MNC derived from an apheresis procedure where the Optia was primed with leukoreduced, ABO-matched whole blood from a heterologous donor (top) or ICS of peripheral blood mononuclear cells (PBMC) isolated from a blood draw taken prior to leukapheresis (bottom). As in panel A, cells were either left unstimulated (“No stim”, left) or stimulated with positive control CMV lysate antigen (“CMV lysate”, right). Plots are gated on CD3+CD4+ singlets.

Article Snippet: Priming blood was leukoreduced using a BPF High Efficiency Leukocyte Reduction Filtration System (Haemonetics, Braintree, MA), which removes both leukocytes and platelets, according to manufacturer’s instructions.

Techniques: Staining, Derivative Assay, Positive Control, Filtration, Cell Counting, Isolation

Mass spectra of metabolites formed during degradation of BPF by strain FM-2. (A) Metabolite I identified as bis(4-hydroxyphenyl)-methanol with trimethylsilylation. (B) Metabolite II identified as DHBP with trimethylsilylation. (C) Metabolite III identified as 1,4-hydroquinone with trimethylsilylation. (D) Metabolite IV identified as 1,4-benzoquinone. (E) Metabolite V identified as 4HB with trimethylsilylation. (F) Metabolite VI tentatively identified as 4-hydroxyphenyl 4-hydroxybenzoate with trimethylsilylation.

Journal:

Article Title: Degradation of Bis(4-Hydroxyphenyl)Methane (Bisphenol F) by Sphingobium yanoikuyae Strain FM-2 Isolated from River Water

doi: 10.1128/AEM.01708-07

Figure Lengend Snippet: Mass spectra of metabolites formed during degradation of BPF by strain FM-2. (A) Metabolite I identified as bis(4-hydroxyphenyl)-methanol with trimethylsilylation. (B) Metabolite II identified as DHBP with trimethylsilylation. (C) Metabolite III identified as 1,4-hydroquinone with trimethylsilylation. (D) Metabolite IV identified as 1,4-benzoquinone. (E) Metabolite V identified as 4HB with trimethylsilylation. (F) Metabolite VI tentatively identified as 4-hydroxyphenyl 4-hydroxybenzoate with trimethylsilylation.

Article Snippet: BPF, tetramethyl BPF (TMBPF), BPE, BPA, BPP, BPB, benzophenone (BP), 4,4′-dihydroxybenzophenone (DHBP), bis(4-hydroxyphenyl)sulfide (TDP), and bis(4-hydroxyphenyl)sulfone (BPS) were purchased from Tokyo Chemical Industry (Tokyo, Japan).

Techniques: