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Endress+Hauser inc dna sequencing gel apparatus
Dna Sequencing Gel Apparatus, supplied by Endress+Hauser 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/product/dna+sequencing+gel+apparatus/dna+sequencing+gel+apparatus/pmc11246215-66-0-10
Average 90 stars, based on 1 article reviews
dna sequencing gel apparatus - by Bioz Stars, 2026-09
90/100 stars

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Incubation:

Article Title: Cleavage of a C-terminal Peptide Is Essential for Heptamerization of Clostridium perfringens ε-Toxin in the Synaptosomal Membrane
Article Snippet: .. After incubation at 37 ̊C for 90 min, SDS sample buffer was added to the reaction mixtures, followed by heating at 95 ̊C for 5 min. To separate heteromeric polymers, SDS-PAGE was performed on a 5% polyacrylamide gel prepared in a DNA sequencing gel apparatus (800 x 170 x 0.4 mm; Bio-Rad, Hercules, Calif.) at 15 mA and room temperature for 20 h. Analytical Methods—N-Terminal amino acid sequencing of the purified toxins was performed with a protein sequencer (model 492 Procise; Applied Biosystems), as described previously (23). .. Protein concentrations were measured using Pierce bicinchoninic acid protein assay reagent (Pierce) with bovine serum albumin as the standard.

SDS Page:

Article Title: Cleavage of a C-terminal Peptide Is Essential for Heptamerization of Clostridium perfringens ε-Toxin in the Synaptosomal Membrane
Article Snippet: .. After incubation at 37 ̊C for 90 min, SDS sample buffer was added to the reaction mixtures, followed by heating at 95 ̊C for 5 min. To separate heteromeric polymers, SDS-PAGE was performed on a 5% polyacrylamide gel prepared in a DNA sequencing gel apparatus (800 x 170 x 0.4 mm; Bio-Rad, Hercules, Calif.) at 15 mA and room temperature for 20 h. Analytical Methods—N-Terminal amino acid sequencing of the purified toxins was performed with a protein sequencer (model 492 Procise; Applied Biosystems), as described previously (23). .. Protein concentrations were measured using Pierce bicinchoninic acid protein assay reagent (Pierce) with bovine serum albumin as the standard.

DNA Sequencing:

Article Title: Cleavage of a C-terminal Peptide Is Essential for Heptamerization of Clostridium perfringens ε-Toxin in the Synaptosomal Membrane
Article Snippet: .. After incubation at 37 ̊C for 90 min, SDS sample buffer was added to the reaction mixtures, followed by heating at 95 ̊C for 5 min. To separate heteromeric polymers, SDS-PAGE was performed on a 5% polyacrylamide gel prepared in a DNA sequencing gel apparatus (800 x 170 x 0.4 mm; Bio-Rad, Hercules, Calif.) at 15 mA and room temperature for 20 h. Analytical Methods—N-Terminal amino acid sequencing of the purified toxins was performed with a protein sequencer (model 492 Procise; Applied Biosystems), as described previously (23). .. Protein concentrations were measured using Pierce bicinchoninic acid protein assay reagent (Pierce) with bovine serum albumin as the standard.

Article Title: New Synthetic Analogs of Nitrogen Mustard DNA Interstrand Crosslinks and Their Use to Study Lesion Bypass by DNA Polymerases
Article Snippet: Polyacrylamide gel electrophoresis (PAGE) supplies and electroelution supplies were purchased from Bio-Rad Laboratories (Hercules, CA, USA). .. DNA sequencing gel apparatus and its supplies were purchased from Analytik Jena AG (Jena, Germany). .. SYBRTM Gold nucleic acid gel stain was purchased from Invitrogen (Carlsbad, CA, USA).

Sequencing:

Article Title: Cleavage of a C-terminal Peptide Is Essential for Heptamerization of Clostridium perfringens ε-Toxin in the Synaptosomal Membrane
Article Snippet: .. After incubation at 37 ̊C for 90 min, SDS sample buffer was added to the reaction mixtures, followed by heating at 95 ̊C for 5 min. To separate heteromeric polymers, SDS-PAGE was performed on a 5% polyacrylamide gel prepared in a DNA sequencing gel apparatus (800 x 170 x 0.4 mm; Bio-Rad, Hercules, Calif.) at 15 mA and room temperature for 20 h. Analytical Methods—N-Terminal amino acid sequencing of the purified toxins was performed with a protein sequencer (model 492 Procise; Applied Biosystems), as described previously (23). .. Protein concentrations were measured using Pierce bicinchoninic acid protein assay reagent (Pierce) with bovine serum albumin as the standard.

Purification:

Article Title: Cleavage of a C-terminal Peptide Is Essential for Heptamerization of Clostridium perfringens ε-Toxin in the Synaptosomal Membrane
Article Snippet: .. After incubation at 37 ̊C for 90 min, SDS sample buffer was added to the reaction mixtures, followed by heating at 95 ̊C for 5 min. To separate heteromeric polymers, SDS-PAGE was performed on a 5% polyacrylamide gel prepared in a DNA sequencing gel apparatus (800 x 170 x 0.4 mm; Bio-Rad, Hercules, Calif.) at 15 mA and room temperature for 20 h. Analytical Methods—N-Terminal amino acid sequencing of the purified toxins was performed with a protein sequencer (model 492 Procise; Applied Biosystems), as described previously (23). .. Protein concentrations were measured using Pierce bicinchoninic acid protein assay reagent (Pierce) with bovine serum albumin as the standard.



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