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- Table of Contents
Facts about Utrophin.
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Human | |
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Gene Name: | UTRN |
Uniprot: | P46939 |
Entrez: | 7402 |
Belongs to: |
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No superfamily |
DMDLutrophin (homologous to dystrophin); DRP; DRP1DRP-1; Dystrophin-related protein 1; FLJ23678; utrophin
Mass (kDA):
394.466 kDA
Human | |
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Location: | 6q24.2 |
Sequence: | 6; NC_000006.12 (144284955..144853034) |
Isoform 1 has high expression in muscle. Isoforms Up70 and Up140 were found in all the adult and fetal tissues tested and relatively abundant in lung and kidney.
Cell junction, synapse, postsynaptic cell membrane; Peripheral membrane protein; Cytoplasmic side. Cytoplasm, cytoskeleton. Neuromuscular junction.
The UTRN Marker is the most widely used peptide marker in the field of biomedical research. This article will cover the history of Boster Bio, the UTRN Marker binding location, how to optimize your ELISA kit and a troubleshooting guide. This article will be useful for both scientists and researchers. It can also serve as a guide for research on samples of different types and in different countries.
Boster Bio stands out when it comes to antibody manufacturing. Its focus on immunohistochemistry and pathology is second to none. Boster Bio's immunohistochemistry service features high throughput screening, confirmation of results, and multiplex IHC. Boster Bio also offers multiplex IHC results archiving at a very affordable price. Boster Bio is known for consistently producing high-quality IHC results.
Steven Boster started developing products in 1993. He was later called "he who converted science in the lavatory". The company was producing hundreds and thousands of primary antibodies, and was the most important catalog antibody company China by the end of the nineties. Boster also invented PicoKine(tm), a proprietary ELISA technology that allows the creation of high-sensitivity ELISA kits. The company also employs proprietary trade secrets to create the PicoKine(tm) platform.
To activate Fushitarazu(Ftz) the UTRN Marker needs to have a TCAATTAAATGA sequencing. This sequence can be changed by one base pair to remove Ftz from binding and activate the gene. Multiple studies have shown Ftz's binding is required for gene transcript. This sequence is called a TATA-binding area.
The homeodomain of a UTRN Marker in eukaryotic cell is similar to one found in bacteriophages. The first helix in this domain is located across the major groove, while the second partially lies within the groove. The recognition helix regulates the sequence specificity and binding activity of proteins to the DNA. The second helix looks similar to the recognition-helix in bacterial cell.
An ELISA experiment involves a number of choices. Optimizing your ELISA will bring up many questions. The ELISA technique will determine the best antibody concentration for your experiment. Other questions that may arise during sample preparation include how to mix blocking buffer and the antibody. The Boster Bio ELISA kit optimization guide can help you sort through these details and ensure that your experiment is as accurate as possible.
A thorough ELISA optimization guide will also cover the basics of immunohistochemistry. It will address common problems, such as low staining and high background. The guide also outlines troubleshooting steps. It also includes a wide range of IHC resources. The BosterBio ELISA Kit Optimization Guide identifies, and describes, the most important IHC methods. While there are many resources for optimizing your assays, the Boster Bio guide provides specific tips that are relevant to the kit you are using.
ELISA optimization is crucial in maximizing the results of your experiments. It is essential to understand the ELISA process, the reagents used and the process of analyzing the results. A good ELISA optimization guide will provide a detailed analysis of the results to help you choose the most effective ELISA. Boster ELISA products have a high-affinity antibody, which detects proteins in the native form. Boster's QC department also validates every ELISA kit with immunogenic protein of relevant superfamilies.
The first step in optimizing an ELISA kit is to choose the species you wish to test. You can choose a direct ELISA kit if you are looking for a fast response and want to avoid the hassle of purifying the antigen. An indirect ELISA Kit is a better option if you're looking for a sensitive and reliable assay. The latter is better for complex samples and doesn't require the purification of the antigen. In addition to ELISA optimization, you can also choose a sandwich ELISA if you are using a sample from a complicated tissue.
A well-optimized ELISA kit should have accurate results. The signal intensity of an ELISA Kit is directly proportional to the amount target protein present in the sample. This makes it possible to compare samples of different batches by their concentrations of the target protein. Alternatively, you can calculate the concentration of the target protein using a standard curve based on known target protein concentrations. Your results can then be used to optimize your ELISA.
Once you are familiar with the basics, it is easy to use the UTRN Marker. There are some issues that can arise, and this guide will help you to resolve them. First, make sure you check that the o rings are still intact. Usually, if they're not, you can just replace them. However, in some cases this may not be possible. In such cases you will need to consult a F1P certified technician.
Hard dives may damage the internal components of the UTRN marker. This could cause the trigger detector to bend. You can fix the problem if this happens. Hold the power button down until the flashing light turns purple. Then, open the battery compartment. Next, locate a small silver box near to the top. Next, bend the box towards you trigger until you hear a click. You can also tighten it with small nuts.
PMID: 1461283 by Tinsley J.M., et al. Primary structure of dystrophin-related protein.
PMID: 10369873 by Wilson J., et al. Up71 and up140, two novel transcripts of utrophin that are homologues of short forms of dystrophin.