DNA Slot Blot Repair Assay —BIO-PROTOCOL Here we describe DNA slot blot repair assay for quantitative detection of NER activity using DNA damage specific antibodies such as anti-CPD and anti-6-4PP. Briefly, genomic DNA irradiated with UV was isolated from cells, and the genomic DNA was vacuum-transferred to a nitrocellulose membrane using a Bio-Dot SF microfiltration apparatus (Bio-Rad). Bio-Dot SF Microfiltration Apparatus Instruction Manual The Bio-Dot SF blotting apparatus has an evenly spaced, slot shaped sample template for easy slot blot sample comparisons. Because the Bio-Dot SF apparatus focuses the applied samples in a thin line instead of a circle, this slot format makes it easy to use a densitometer to quantitate results. Western Blot Protocol | Bio-Rad This western blot protocol provides a general procedure for use with the majority of Bio-Rad reagents. In some cases specific recommendations are provided on product datasheets, and these methods should always be used in conjunction with product and batch specific information provided with each vial. and Bio-Dot SF Microfiltration Apparatus - bio-rad.com
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RNA BIO-DOT (‘SLOT BLOT’) Adapted from existing protocols by Vinh Pham. Last modified: July 8, 2003 MATERIALS: DRY Bio-Rad Bio-Dot SF Microfiltration Apparatus Nytran membrane Bio-Dot SF filter paper 60 DNA Slot Blot Repair Assay [Abstract] - Bio-protocol removes UV-induced DNA damages. Here we describe DNA slot blot repair assay for quantitative detection of NER activity using damage specific antibodies such as antiDNA -CPD and anti-6-4PP. Briefly, genomic DNA irradiated with UV was isolated from cells, and the genomic DNA was vacuum- Dot blot - Wikipedia A dot blot (or slot blot) is a technique in molecular biology used to detect proteins. It represents a simplification of the western blot method, with the exception that the proteins to be detected are not first separated by electrophoresis.Instead, the sample is applied directly on a membrane in a single spot, and the blotting procedure is performed. Test Blots, Slot Blots & Dot Blots - Immunodetection | Bio-Rad Each dot or slot blot would contain known amounts of target protein or cell lysate. Once dry, dot blots and slot blots are subjected to the same immunodetection steps used for Western blotting, i.e. blocking, antibody incubation, and target detection with substrate.
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Bio-Rad Laboratories warrants the Trans-Blot SD semi-dry electrophoretic transfer cell against defects in materials and workmanship for 1 year. If any defects occur in the instrument during this warranty period, Bio-Rad Laboratories will repair or replace the defective parts free. The following defects, however, are specifically excluded: 1. Western blot protocol - Creative BioMart Fig. The schematic diagram of western bolt protocol. Western blot protocol procedure. Sample prepare. Usually, samples are resuspended or mixed in 20-50 µl of 1X sample buffer and all the mixtures are incubated at 90°C for five minutes or 50°C for 15 minutes to break down the interactions between peptides. A Guide to Transfer and Detection - Potts Lab This reference manual provides information on the fundamentals of protein transfer and detection chemistries. It is also a guide to the methods, equipment, and reagents used ... Turn to Bio-Rad for: • Gel-blotting equipment for an array of gel sizes ... For detailed protocols on the use of any of the products mentioned in this guide, please ... Dot Blot Laboratory Protocol - UF CPET Dot Blot Laboratory Protocol The dot blot is a technique for detecting, analyzing, and identifying proteins, similar to the western blot technique. The dot blot differs from the western in that the protein samples are not separated electrophoretically but are spotted through circular templates directly onto the membrane or paper substrate.
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Bio-Dot SF Microfiltration Apparatus Instruction Manual The Bio-Dot SF blotting apparatus has an evenly spaced, slot shaped sample template for easy slot blot sample comparisons. Because the Bio-Dot SF apparatus focuses the applied samples in a thin line instead of a circle, this slot format makes it easy to use a densitometer to quantitate results. PROTEIN BIO-DOT (‘SLOT BLOT’) - University of California ... 20. Measure [protein] by Lowry method using Bio-Rad DC Protein Assay. Part II – Slot Blotting 1. Cut nitrocellulose membrane and 3 pieces of Whatman paper (use more if bleeding of samples is a problem) to size of Bio-Dot SF filter paper 60. 2. Soak membrane and filter papers in TBS. 3. Touch membrane on dry filter paper to wick off excess ... Test Blots, Slot Blots & Dot Blots - Immunodetection | Bio-Rad Each dot or slot blot would contain known amounts of target protein or cell lysate. Once dry, dot blots and slot blots are subjected to the same immunodetection steps used for Western blotting, i.e. blocking, antibody incubation, and target detection with substrate.
Article Title: Functional and comparative genomic analyses of an operon involved in fructooligosaccharide utilization by Lactobacillus acidophilus Article Snippet: For RNA slot blots, RNA samples were transferred to nitrocellulose membranes (Bio-Rad) using a slot-blot apparatus (Bio-Dot SF, Bio-Rad), and the RNAs were UV crosslinked to the membranes. ..
Western Blot Protocol Western Blot Protocol (8/19/2002). 1.Preparing the sample: -Cutting 20 um frozen sections to a slide, 3-5 of them; depends on the tissue size.Maneuver the gel with forceps or gloved hands to minimize background) -Fill the Bio-Ice cooling unit with water and store it in –20C until ready to use. Anti-RNA blotting with chemiluminescent detection This protocol is for northern blotting/dot-blotting to detect specific RNAs via chemiluminescence, using biotinylated DNA oligo probes.Positively charged nylon membrane (BrightStar-Plus Positively Charged Nylon Membrane, or Roche 11-209-299-001, or Bio-Rad Zeta-Probe #1620154). Western Blot Protocol
DNA Slot Blot Repair Assay —BIO-PROTOCOL Apr 20, 2015 · Here we describe DNA slot blot repair assay for quantitative detection of NER activity using DNA damage specific antibodies such as anti-CPD and anti-6-4PP. Briefly, genomic DNA irradiated with UV was isolated from cells, and the genomic DNA was vacuum-transferred to a nitrocellulose membrane using a Bio-Dot SF microfiltration apparatus (Bio-Rad).