exponential function fit with”exp1 Search Results


ecori bamhi digested exp1 insert  (New England Biolabs)
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anti crm1 antibody  (Proteintech)
93
Proteintech anti crm1 antibody
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function fit with fittype: exp1  (MathWorks Inc)
90
MathWorks Inc function fit with fittype: exp1
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top2b chipseq  (Novus Biologicals)
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tubulin exp1 antibody  (Novus Biologicals)
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Novus Biologicals tubulin exp1 antibody
Tubulin Exp1 Antibody, supplied by Novus Biologicals, 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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klh-conjugated peptides of exp1  (GL Biochem)
90
GL Biochem klh-conjugated peptides of exp1
(A) Infected HepG2 cultures fixed at 65 hpi, were immunostained with the PVM markers anti-UIS4 and <t>anti-EXP1</t> antibodies. Nuclei were stained with Hoechst. ( B and C) Intact and ruptured PVMs were quantified, and we detected a significantly greater number of EEFs with intact PVMs in UIS28 KO than in WT GFP immunostained with anti-UIS4 (****P<0.0001) and anti-EXP1 (**P=0.0068). The data were obtained from multiple coverslips and are presented as the mean ± SD. Statistical significance was determined by one-way ANOVA. (D) Infected cultures fixed at 65 hpi were immunostained with an anti-β-actin antibody. Nuclei were stained with Hoechst. Different types of actin localization patterns (condensed/dotted, absent, or associated with the plasma membrane) in infected cells were quantified. (E) Quantification of the actin localization pattern in infected cells. We detected a greater percentage of plasma membrane-associated actin in KO parasites than in WT parasites (*P=0.0162, Students t test). The other actin patterns were similar in both groups. A total of 72 (WT GFP) and 112 (UIS28 KO) EEFs were analyzed. Data were pooled from two independent experiments and are shown as the mean ± SD.
Klh Conjugated Peptides Of Exp1, supplied by GL Biochem, 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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rat anti-exp1  (ProteoGenix)
90
ProteoGenix rat anti-exp1
(A) Infected HepG2 cultures fixed at 65 hpi, were immunostained with the PVM markers anti-UIS4 and <t>anti-EXP1</t> antibodies. Nuclei were stained with Hoechst. ( B and C) Intact and ruptured PVMs were quantified, and we detected a significantly greater number of EEFs with intact PVMs in UIS28 KO than in WT GFP immunostained with anti-UIS4 (****P<0.0001) and anti-EXP1 (**P=0.0068). The data were obtained from multiple coverslips and are presented as the mean ± SD. Statistical significance was determined by one-way ANOVA. (D) Infected cultures fixed at 65 hpi were immunostained with an anti-β-actin antibody. Nuclei were stained with Hoechst. Different types of actin localization patterns (condensed/dotted, absent, or associated with the plasma membrane) in infected cells were quantified. (E) Quantification of the actin localization pattern in infected cells. We detected a greater percentage of plasma membrane-associated actin in KO parasites than in WT parasites (*P=0.0162, Students t test). The other actin patterns were similar in both groups. A total of 72 (WT GFP) and 112 (UIS28 KO) EEFs were analyzed. Data were pooled from two independent experiments and are shown as the mean ± SD.
Rat Anti Exp1, supplied by ProteoGenix, 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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exp1 antigen  (Broad Institute Inc)
90
Broad Institute Inc exp1 antigen
(A) Infected HepG2 cultures fixed at 65 hpi, were immunostained with the PVM markers anti-UIS4 and <t>anti-EXP1</t> antibodies. Nuclei were stained with Hoechst. ( B and C) Intact and ruptured PVMs were quantified, and we detected a significantly greater number of EEFs with intact PVMs in UIS28 KO than in WT GFP immunostained with anti-UIS4 (****P<0.0001) and anti-EXP1 (**P=0.0068). The data were obtained from multiple coverslips and are presented as the mean ± SD. Statistical significance was determined by one-way ANOVA. (D) Infected cultures fixed at 65 hpi were immunostained with an anti-β-actin antibody. Nuclei were stained with Hoechst. Different types of actin localization patterns (condensed/dotted, absent, or associated with the plasma membrane) in infected cells were quantified. (E) Quantification of the actin localization pattern in infected cells. We detected a greater percentage of plasma membrane-associated actin in KO parasites than in WT parasites (*P=0.0162, Students t test). The other actin patterns were similar in both groups. A total of 72 (WT GFP) and 112 (UIS28 KO) EEFs were analyzed. Data were pooled from two independent experiments and are shown as the mean ± SD.
Exp1 Antigen, supplied by Broad Institute 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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function exp1  (MathWorks Inc)
90
MathWorks Inc function exp1
(A) Infected HepG2 cultures fixed at 65 hpi, were immunostained with the PVM markers anti-UIS4 and <t>anti-EXP1</t> antibodies. Nuclei were stained with Hoechst. ( B and C) Intact and ruptured PVMs were quantified, and we detected a significantly greater number of EEFs with intact PVMs in UIS28 KO than in WT GFP immunostained with anti-UIS4 (****P<0.0001) and anti-EXP1 (**P=0.0068). The data were obtained from multiple coverslips and are presented as the mean ± SD. Statistical significance was determined by one-way ANOVA. (D) Infected cultures fixed at 65 hpi were immunostained with an anti-β-actin antibody. Nuclei were stained with Hoechst. Different types of actin localization patterns (condensed/dotted, absent, or associated with the plasma membrane) in infected cells were quantified. (E) Quantification of the actin localization pattern in infected cells. We detected a greater percentage of plasma membrane-associated actin in KO parasites than in WT parasites (*P=0.0162, Students t test). The other actin patterns were similar in both groups. A total of 72 (WT GFP) and 112 (UIS28 KO) EEFs were analyzed. Data were pooled from two independent experiments and are shown as the mean ± SD.
Function Exp1, supplied by MathWorks 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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mzrtree  (Chrom Tech)
90
Chrom Tech mzrtree
(A) Infected HepG2 cultures fixed at 65 hpi, were immunostained with the PVM markers anti-UIS4 and <t>anti-EXP1</t> antibodies. Nuclei were stained with Hoechst. ( B and C) Intact and ruptured PVMs were quantified, and we detected a significantly greater number of EEFs with intact PVMs in UIS28 KO than in WT GFP immunostained with anti-UIS4 (****P<0.0001) and anti-EXP1 (**P=0.0068). The data were obtained from multiple coverslips and are presented as the mean ± SD. Statistical significance was determined by one-way ANOVA. (D) Infected cultures fixed at 65 hpi were immunostained with an anti-β-actin antibody. Nuclei were stained with Hoechst. Different types of actin localization patterns (condensed/dotted, absent, or associated with the plasma membrane) in infected cells were quantified. (E) Quantification of the actin localization pattern in infected cells. We detected a greater percentage of plasma membrane-associated actin in KO parasites than in WT parasites (*P=0.0162, Students t test). The other actin patterns were similar in both groups. A total of 72 (WT GFP) and 112 (UIS28 KO) EEFs were analyzed. Data were pooled from two independent experiments and are shown as the mean ± SD.
Mzrtree, supplied by Chrom Tech, 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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fit function with the 'exp1' parameter  (MathWorks Inc)
90
MathWorks Inc fit function with the 'exp1' parameter
(A) Infected HepG2 cultures fixed at 65 hpi, were immunostained with the PVM markers anti-UIS4 and <t>anti-EXP1</t> antibodies. Nuclei were stained with Hoechst. ( B and C) Intact and ruptured PVMs were quantified, and we detected a significantly greater number of EEFs with intact PVMs in UIS28 KO than in WT GFP immunostained with anti-UIS4 (****P<0.0001) and anti-EXP1 (**P=0.0068). The data were obtained from multiple coverslips and are presented as the mean ± SD. Statistical significance was determined by one-way ANOVA. (D) Infected cultures fixed at 65 hpi were immunostained with an anti-β-actin antibody. Nuclei were stained with Hoechst. Different types of actin localization patterns (condensed/dotted, absent, or associated with the plasma membrane) in infected cells were quantified. (E) Quantification of the actin localization pattern in infected cells. We detected a greater percentage of plasma membrane-associated actin in KO parasites than in WT parasites (*P=0.0162, Students t test). The other actin patterns were similar in both groups. A total of 72 (WT GFP) and 112 (UIS28 KO) EEFs were analyzed. Data were pooled from two independent experiments and are shown as the mean ± SD.
Fit Function With The 'exp1' Parameter, supplied by MathWorks 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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anti-exp1  (Becton Dickinson)
90
Becton Dickinson anti-exp1
(A) Infected HepG2 cultures fixed at 65 hpi, were immunostained with the PVM markers anti-UIS4 and <t>anti-EXP1</t> antibodies. Nuclei were stained with Hoechst. ( B and C) Intact and ruptured PVMs were quantified, and we detected a significantly greater number of EEFs with intact PVMs in UIS28 KO than in WT GFP immunostained with anti-UIS4 (****P<0.0001) and anti-EXP1 (**P=0.0068). The data were obtained from multiple coverslips and are presented as the mean ± SD. Statistical significance was determined by one-way ANOVA. (D) Infected cultures fixed at 65 hpi were immunostained with an anti-β-actin antibody. Nuclei were stained with Hoechst. Different types of actin localization patterns (condensed/dotted, absent, or associated with the plasma membrane) in infected cells were quantified. (E) Quantification of the actin localization pattern in infected cells. We detected a greater percentage of plasma membrane-associated actin in KO parasites than in WT parasites (*P=0.0162, Students t test). The other actin patterns were similar in both groups. A total of 72 (WT GFP) and 112 (UIS28 KO) EEFs were analyzed. Data were pooled from two independent experiments and are shown as the mean ± SD.
Anti Exp1, supplied by Becton Dickinson, 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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Image Search Results


(A) Infected HepG2 cultures fixed at 65 hpi, were immunostained with the PVM markers anti-UIS4 and anti-EXP1 antibodies. Nuclei were stained with Hoechst. ( B and C) Intact and ruptured PVMs were quantified, and we detected a significantly greater number of EEFs with intact PVMs in UIS28 KO than in WT GFP immunostained with anti-UIS4 (****P<0.0001) and anti-EXP1 (**P=0.0068). The data were obtained from multiple coverslips and are presented as the mean ± SD. Statistical significance was determined by one-way ANOVA. (D) Infected cultures fixed at 65 hpi were immunostained with an anti-β-actin antibody. Nuclei were stained with Hoechst. Different types of actin localization patterns (condensed/dotted, absent, or associated with the plasma membrane) in infected cells were quantified. (E) Quantification of the actin localization pattern in infected cells. We detected a greater percentage of plasma membrane-associated actin in KO parasites than in WT parasites (*P=0.0162, Students t test). The other actin patterns were similar in both groups. A total of 72 (WT GFP) and 112 (UIS28 KO) EEFs were analyzed. Data were pooled from two independent experiments and are shown as the mean ± SD.

Journal: bioRxiv

Article Title: A Plasmodium lipase is critical for the disruption of the parasitophorous vacuole membrane and egress of hepatic merozoites

doi: 10.1101/2025.06.02.657352

Figure Lengend Snippet: (A) Infected HepG2 cultures fixed at 65 hpi, were immunostained with the PVM markers anti-UIS4 and anti-EXP1 antibodies. Nuclei were stained with Hoechst. ( B and C) Intact and ruptured PVMs were quantified, and we detected a significantly greater number of EEFs with intact PVMs in UIS28 KO than in WT GFP immunostained with anti-UIS4 (****P<0.0001) and anti-EXP1 (**P=0.0068). The data were obtained from multiple coverslips and are presented as the mean ± SD. Statistical significance was determined by one-way ANOVA. (D) Infected cultures fixed at 65 hpi were immunostained with an anti-β-actin antibody. Nuclei were stained with Hoechst. Different types of actin localization patterns (condensed/dotted, absent, or associated with the plasma membrane) in infected cells were quantified. (E) Quantification of the actin localization pattern in infected cells. We detected a greater percentage of plasma membrane-associated actin in KO parasites than in WT parasites (*P=0.0162, Students t test). The other actin patterns were similar in both groups. A total of 72 (WT GFP) and 112 (UIS28 KO) EEFs were analyzed. Data were pooled from two independent experiments and are shown as the mean ± SD.

Article Snippet: KLH-conjugated peptides of EXP1 (KNKHGKTGSKNVIKKP-Cys) was synthesized by GL Biochem (Shanghai) Ltd.

Techniques: Infection, Staining, Clinical Proteomics, Membrane