QUESTION 11Below is a diagram of an assay you learned a lot about in class. In the third image, what is the little purple ball near the top supposed to represent?1O AnalyteO a patient sampleO An enzymeO A substrateA virusO An antibody2.

The biological capacity of antibodies is to tie to microbes and their products, and to work with…

Answered: low is a diagram of an assay you…

Human Anatomy & Physiology (11th Edition)

11th Edition

ISBN:9780134580999

Author:Elaine N. Marieb, Katja N. Hoehn

Publisher:Elaine N. Marieb, Katja N. Hoehn

Chapter1: The Human Body: An Orientation

Section: Chapter Questions

Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...

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Similar questions

Why amplify DNA using PCR before doing electrophoresis? Why not just take your DNA sample and directly run a gel?
A health provider contacts you regarding a specific patient. They ask you to sequence this patient’s DNA and sends you her blood sample. You split the patient’s blood sample into three equal parts. With each part, you perform three different protocols of DNA extraction and purification. You analyze the resulting DNA using the nanodrop. Protocol A260/280 ng/ul DNA Total volume (ul) 1 2.02 50 60 2 1.45 156 200 3 0.30 300 120 d)Halfway through the electrophoresis of your gel you realized that rather than using a buffer to make up your gel, you actually used distilled water. Do you think this mistake would alter the outcome of your gel electrophoresis? Explain. e) If you added your DNA to a well in a gel without first mixing it with gel loading solution, would this impact the final results? Explain. f) Only after the run you realize that you forgot to add ethidium bromide to the gel. What will happen to your sample? What could you do to the gel after the run?
Hello which one can be the right answer?
Give information about the microchip that could control drugs invented by Robert Langer and Michael Cima. When the studies started, how did the idea come out, who found it, which university the studies were carried out, what exactly does the product work, when was the patent obtained? Write important information about this polymer wafer (Please don't give short answer)
DNA is visualized during agarose gel electrophoresis by ______________ . the fact that DNA fluoresces when illuminated with UV light the binding of a fluorescent dye that is easily detectable using radioactive antibodies that specifically bind to DNA the fact that DNA is blue and can be seen when millions of copies are present in a band
Give a detailed description of how probes are designed and arranged on a resequencing array. Your description should include the size (in base pairs) of the probe, where differences in sequence are located within the probe, and the types of experiments that would use this type of microarray.
DNA Cheek Cells Lab Identify the component of the solution which is the extracted DNA
A student is trying to add 9.0 pmol of primer mix to a 20.0 µL PCR. The primer mix is at a concentration of 50.0 µM, and the student determines that a serial dilution is required because directly adding the primer mix would require a volume less than 1.00 µL. The student takes 1.40 µL of the primer mix stock and mixes it with 25.0 µL of ultrapure H2O. Calculate the volume (in µL) of the intermediate solution required to add the correct amount of primer mix to the PCR.
You are given a tube containing 275 ng of purified PCR product (DNA) that is 1262 bp long. How many picomoles of PCR product are in the tube? The average molecular weight of a deoxynucleotide monophosphate is 328 g/mol.
What does it mean for viral DNA to program cells? explain in your own words as simply as possible.
Which organism would be your first choice for transformation: a bacterium, earthworm, fish or mouse? Describe your reasoning
You are trying to determine the base content for a number of samples in the lab (mouse DNA, bacterial DNA, single-stranded DNA virus and double-stranded RNA virus). Unfortunately, you failed to use an alcohol-proof marker and during the ethanol precipitation of your samples the labels came off the tubes. You finish the experiment anyway and try to use the data to determine the samples. Can you determine the source of each sample based on your results? Briefly explain how you come to your designations. Sample % adenine % cytosine % guanine % thymine % uracil A 18 32 32 18 0 B 26 18 32 24 0 C 31 19 19 0 31 D 10 40 40 10 0

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low is a diagram of an assay you learned a lot about in class. In the third image, what is the little purple ball near the top supposed to represent? 4 Analyte a patient sample An enzyme A substrate A virus An antibody