43296 Search Results


p limnophila atcc 43296  (ATCC)
92
ATCC p limnophila atcc 43296
P Limnophila Atcc 43296, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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aryl alcohol dehydrogenase gene  (DSMZ)
92
DSMZ aryl alcohol dehydrogenase gene
Aryl Alcohol Dehydrogenase Gene, supplied by DSMZ, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bm dsm3120  (DSMZ)
90
DSMZ bm dsm3120
Origin of Basidiobolus isolates used in the present study and GenBank accession numbers of the submitted 18S rRNA (SSU) and partial 28S rRNA (LSU, D1/D2 domain) gene sequences.
Bm Dsm3120, supplied by DSMZ, 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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transam tf elisa kit 43296  (Active Motif)
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Active Motif transam tf elisa kit 43296
Origin of Basidiobolus isolates used in the present study and GenBank accession numbers of the submitted 18S rRNA (SSU) and partial 28S rRNA (LSU, D1/D2 domain) gene sequences.
Transam Tf Elisa Kit 43296, supplied by Active Motif, 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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enzyme-linked immunosorbent assay kit number 43296  (Active Motif)
90
Active Motif enzyme-linked immunosorbent assay kit number 43296
Quantitative real-time polymerase chain reaction analyzed (a) Il-1β, (b) TGF-β, and (c) TNF mRNA level in HK-2 cells transfected with ANXA1 small, interfering RNA (siRNA) under high glucose plus palmitic acid (HGPA) conditions. n = 4 per group. (d) Top: Representative Western blot images. Bottom: Analyses of phosphorylated p65 (p-p65) and p65 in HK-2 cells with treatment. n = 3 per group. (e) Top: Total protein lysates of HK-2 cells treated with HGPA or siRNA against ANXA1 (siANXA1) were immunoprecipitated using an antibody against the p65 subunit of NF-κB and immunoblotted (IB) against ANXA1. Bottom: Total protein lysates of HK-2 cells treated with HGPA or siANXA1 were immunoprecipitated using an antibody against ANXA1 and IB against the p65 subunit of NF-κB. (f) The surface plasmon resonance (SPR) curves generated from ANXA1 binding to p65. The ANXA1 protein concentration ranged from 7.8 to 250 nM. The apparent dissociation constants for the interaction were obtained from fitting the SPR response curves to a simple 1:1 Langmuir binding model. (g) Electrophoretic mobility shift assay showed the binding of NF-κB to the DNA probe in HK-2 cells under different treatments. (h) Enzyme-linked <t>immunosorbent</t> assay showed the NF-κB activity as indicated. n = 3 per group. Data analysis was performed by Student t test for 2 groups and 2-way analysis of variance, followed by a Tukey test, for multiple groups and expressed as mean ± SD. The blank group served as the normal control group. The control group served as the isotonic solvent control group using mannitol and endotoxin-free bovine serum albumin. *P < 0.05, **P < 0.01, and ***P < 0.001. GAPDH, glyceraldehyde 3-phosphate dehydrogenase; siCtrl, negative control siRNA.
Enzyme Linked Immunosorbent Assay Kit Number 43296, supplied by Active Motif, 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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assay #43296  (Active Motif)
90
Active Motif assay #43296
Quantitative real-time polymerase chain reaction analyzed (a) Il-1β, (b) TGF-β, and (c) TNF mRNA level in HK-2 cells transfected with ANXA1 small, interfering RNA (siRNA) under high glucose plus palmitic acid (HGPA) conditions. n = 4 per group. (d) Top: Representative Western blot images. Bottom: Analyses of phosphorylated p65 (p-p65) and p65 in HK-2 cells with treatment. n = 3 per group. (e) Top: Total protein lysates of HK-2 cells treated with HGPA or siRNA against ANXA1 (siANXA1) were immunoprecipitated using an antibody against the p65 subunit of NF-κB and immunoblotted (IB) against ANXA1. Bottom: Total protein lysates of HK-2 cells treated with HGPA or siANXA1 were immunoprecipitated using an antibody against ANXA1 and IB against the p65 subunit of NF-κB. (f) The surface plasmon resonance (SPR) curves generated from ANXA1 binding to p65. The ANXA1 protein concentration ranged from 7.8 to 250 nM. The apparent dissociation constants for the interaction were obtained from fitting the SPR response curves to a simple 1:1 Langmuir binding model. (g) Electrophoretic mobility shift assay showed the binding of NF-κB to the DNA probe in HK-2 cells under different treatments. (h) Enzyme-linked <t>immunosorbent</t> assay showed the NF-κB activity as indicated. n = 3 per group. Data analysis was performed by Student t test for 2 groups and 2-way analysis of variance, followed by a Tukey test, for multiple groups and expressed as mean ± SD. The blank group served as the normal control group. The control group served as the isotonic solvent control group using mannitol and endotoxin-free bovine serum albumin. *P < 0.05, **P < 0.01, and ***P < 0.001. GAPDH, glyceraldehyde 3-phosphate dehydrogenase; siCtrl, negative control siRNA.
Assay #43296, supplied by Active Motif, 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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elisa transam nfjb family #43296  (Active Motif)
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Active Motif elisa transam nfjb family #43296
Quantitative real-time polymerase chain reaction analyzed (a) Il-1β, (b) TGF-β, and (c) TNF mRNA level in HK-2 cells transfected with ANXA1 small, interfering RNA (siRNA) under high glucose plus palmitic acid (HGPA) conditions. n = 4 per group. (d) Top: Representative Western blot images. Bottom: Analyses of phosphorylated p65 (p-p65) and p65 in HK-2 cells with treatment. n = 3 per group. (e) Top: Total protein lysates of HK-2 cells treated with HGPA or siRNA against ANXA1 (siANXA1) were immunoprecipitated using an antibody against the p65 subunit of NF-κB and immunoblotted (IB) against ANXA1. Bottom: Total protein lysates of HK-2 cells treated with HGPA or siANXA1 were immunoprecipitated using an antibody against ANXA1 and IB against the p65 subunit of NF-κB. (f) The surface plasmon resonance (SPR) curves generated from ANXA1 binding to p65. The ANXA1 protein concentration ranged from 7.8 to 250 nM. The apparent dissociation constants for the interaction were obtained from fitting the SPR response curves to a simple 1:1 Langmuir binding model. (g) Electrophoretic mobility shift assay showed the binding of NF-κB to the DNA probe in HK-2 cells under different treatments. (h) Enzyme-linked <t>immunosorbent</t> assay showed the NF-κB activity as indicated. n = 3 per group. Data analysis was performed by Student t test for 2 groups and 2-way analysis of variance, followed by a Tukey test, for multiple groups and expressed as mean ± SD. The blank group served as the normal control group. The control group served as the isotonic solvent control group using mannitol and endotoxin-free bovine serum albumin. *P < 0.05, **P < 0.01, and ***P < 0.001. GAPDH, glyceraldehyde 3-phosphate dehydrogenase; siCtrl, negative control siRNA.
Elisa Transam Nfjb Family #43296, supplied by Active Motif, 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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transamnf-κb family kit cat. no: 43296  (Active Motif)
90
Active Motif transamnf-κb family kit cat. no: 43296
Quantitative real-time polymerase chain reaction analyzed (a) Il-1β, (b) TGF-β, and (c) TNF mRNA level in HK-2 cells transfected with ANXA1 small, interfering RNA (siRNA) under high glucose plus palmitic acid (HGPA) conditions. n = 4 per group. (d) Top: Representative Western blot images. Bottom: Analyses of phosphorylated p65 (p-p65) and p65 in HK-2 cells with treatment. n = 3 per group. (e) Top: Total protein lysates of HK-2 cells treated with HGPA or siRNA against ANXA1 (siANXA1) were immunoprecipitated using an antibody against the p65 subunit of NF-κB and immunoblotted (IB) against ANXA1. Bottom: Total protein lysates of HK-2 cells treated with HGPA or siANXA1 were immunoprecipitated using an antibody against ANXA1 and IB against the p65 subunit of NF-κB. (f) The surface plasmon resonance (SPR) curves generated from ANXA1 binding to p65. The ANXA1 protein concentration ranged from 7.8 to 250 nM. The apparent dissociation constants for the interaction were obtained from fitting the SPR response curves to a simple 1:1 Langmuir binding model. (g) Electrophoretic mobility shift assay showed the binding of NF-κB to the DNA probe in HK-2 cells under different treatments. (h) Enzyme-linked <t>immunosorbent</t> assay showed the NF-κB activity as indicated. n = 3 per group. Data analysis was performed by Student t test for 2 groups and 2-way analysis of variance, followed by a Tukey test, for multiple groups and expressed as mean ± SD. The blank group served as the normal control group. The control group served as the isotonic solvent control group using mannitol and endotoxin-free bovine serum albumin. *P < 0.05, **P < 0.01, and ***P < 0.001. GAPDH, glyceraldehyde 3-phosphate dehydrogenase; siCtrl, negative control siRNA.
Transamnf κb Family Kit Cat. No: 43296, supplied by Active Motif, 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


Origin of Basidiobolus isolates used in the present study and GenBank accession numbers of the submitted 18S rRNA (SSU) and partial 28S rRNA (LSU, D1/D2 domain) gene sequences.

Journal: Journal of Fungi

Article Title: Differentiation of Basidiobolus spp. Isolates: RFLP of a Diagnostic PCR Amplicon Matches Sequence-Based Classification and Growth Temperature Preferences

doi: 10.3390/jof7020110

Figure Lengend Snippet: Origin of Basidiobolus isolates used in the present study and GenBank accession numbers of the submitted 18S rRNA (SSU) and partial 28S rRNA (LSU, D1/D2 domain) gene sequences.

Article Snippet: Bm DSM3120 , SSU: MW127176 , , , Culture collection DSMZ, Germany , Type strain.

Techniques:

Quantitative real-time polymerase chain reaction analyzed (a) Il-1β, (b) TGF-β, and (c) TNF mRNA level in HK-2 cells transfected with ANXA1 small, interfering RNA (siRNA) under high glucose plus palmitic acid (HGPA) conditions. n = 4 per group. (d) Top: Representative Western blot images. Bottom: Analyses of phosphorylated p65 (p-p65) and p65 in HK-2 cells with treatment. n = 3 per group. (e) Top: Total protein lysates of HK-2 cells treated with HGPA or siRNA against ANXA1 (siANXA1) were immunoprecipitated using an antibody against the p65 subunit of NF-κB and immunoblotted (IB) against ANXA1. Bottom: Total protein lysates of HK-2 cells treated with HGPA or siANXA1 were immunoprecipitated using an antibody against ANXA1 and IB against the p65 subunit of NF-κB. (f) The surface plasmon resonance (SPR) curves generated from ANXA1 binding to p65. The ANXA1 protein concentration ranged from 7.8 to 250 nM. The apparent dissociation constants for the interaction were obtained from fitting the SPR response curves to a simple 1:1 Langmuir binding model. (g) Electrophoretic mobility shift assay showed the binding of NF-κB to the DNA probe in HK-2 cells under different treatments. (h) Enzyme-linked immunosorbent assay showed the NF-κB activity as indicated. n = 3 per group. Data analysis was performed by Student t test for 2 groups and 2-way analysis of variance, followed by a Tukey test, for multiple groups and expressed as mean ± SD. The blank group served as the normal control group. The control group served as the isotonic solvent control group using mannitol and endotoxin-free bovine serum albumin. *P < 0.05, **P < 0.01, and ***P < 0.001. GAPDH, glyceraldehyde 3-phosphate dehydrogenase; siCtrl, negative control siRNA.

Journal: Kidney international

Article Title: Annexin A1 alleviates kidney injury by promoting the resolution of inflammation in diabetic nephropathy

doi: 10.1016/j.kint.2021.02.025

Figure Lengend Snippet: Quantitative real-time polymerase chain reaction analyzed (a) Il-1β, (b) TGF-β, and (c) TNF mRNA level in HK-2 cells transfected with ANXA1 small, interfering RNA (siRNA) under high glucose plus palmitic acid (HGPA) conditions. n = 4 per group. (d) Top: Representative Western blot images. Bottom: Analyses of phosphorylated p65 (p-p65) and p65 in HK-2 cells with treatment. n = 3 per group. (e) Top: Total protein lysates of HK-2 cells treated with HGPA or siRNA against ANXA1 (siANXA1) were immunoprecipitated using an antibody against the p65 subunit of NF-κB and immunoblotted (IB) against ANXA1. Bottom: Total protein lysates of HK-2 cells treated with HGPA or siANXA1 were immunoprecipitated using an antibody against ANXA1 and IB against the p65 subunit of NF-κB. (f) The surface plasmon resonance (SPR) curves generated from ANXA1 binding to p65. The ANXA1 protein concentration ranged from 7.8 to 250 nM. The apparent dissociation constants for the interaction were obtained from fitting the SPR response curves to a simple 1:1 Langmuir binding model. (g) Electrophoretic mobility shift assay showed the binding of NF-κB to the DNA probe in HK-2 cells under different treatments. (h) Enzyme-linked immunosorbent assay showed the NF-κB activity as indicated. n = 3 per group. Data analysis was performed by Student t test for 2 groups and 2-way analysis of variance, followed by a Tukey test, for multiple groups and expressed as mean ± SD. The blank group served as the normal control group. The control group served as the isotonic solvent control group using mannitol and endotoxin-free bovine serum albumin. *P < 0.05, **P < 0.01, and ***P < 0.001. GAPDH, glyceraldehyde 3-phosphate dehydrogenase; siCtrl, negative control siRNA.

Article Snippet: The activity of nuclear factor (NF)-κB p65 was assessed using an enzyme-linked immunosorbent assay kit (number 43296; Active Motif).

Techniques: Real-time Polymerase Chain Reaction, Transfection, Small Interfering RNA, Western Blot, Immunoprecipitation, SPR Assay, Generated, Binding Assay, Protein Concentration, Electrophoretic Mobility Shift Assay, Enzyme-linked Immunosorbent Assay, Activity Assay, Negative Control