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- Table of Contents
Facts about Peptidyl-prolyl cis-trans isomerase G.
May play an important role in the regulation of pre-mRNA splicing. .
Human | |
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Gene Name: | PPIG |
Uniprot: | Q13427 |
Entrez: | 9360 |
Belongs to: |
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No superfamily |
CARS-cyclophilin; CARS-CypPPIase G; CASP10; Clk-associating RS-cyclophilin; Cyclophilin G; CYP; EC 5.2.1.8; MGC133241; peptidyl-prolyl cis-trans isomerase G; peptidylprolyl isomerase G (cyclophilin G); peptidyl-prolyl isomerase G (cyclophilin G); Peptidyl-prolyl isomerase G; Rotamase G; SCAF10; SR-cyclophilin; SRCyp; SR-cyp; SR-related CTD-associated factor 10
Mass (kDA):
88.617 kDA
Human | |
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Location: | 2q31.1 |
Sequence: | 2; NC_000002.12 (169584343..169641406) |
Ubiquitous.
Nucleus matrix. Nucleus speckle. Colocalizes with RNA splicing factors at nuclear speckles.
A good DNA marker can make a big difference. However, if you're unsure about the Boster Bio and how to use it properly, here are some useful tips. There are also guides to help you analyze your experiments. You'll be surprised by how many benefits you can get from this DNA marker. Read on to find out how BosterBio can be used to your advantage.
To detect the presence of phosphorylatedPPIG antibodies, you can use antibodies for the marker PPIG. Boster Bio offers antibodies that have been validated and cited over the past 25 years. Boster Bio Anti-HumanCD8a Monoclonal Antibody is capable of staining approximately one million cells per uL. This antibody should keep at -20°C. It can also stored at room temperatures for one month.
Boster Bio Anti-TNF Alpha Monoclonal antibodies can react with human, rabbit, and mouse TNF. This product is able to identify many proteins in vitro and vivo. Because of its multifunctionality the EDN1 marker is very useful in biological research. It is a master regulator of phenotype heterogeneity. It can be used as a target gene.
Designed for high affinity protein binding, Boster antibodies have earned trust and respect in the scientific community. Boster antibodies have excellent reviews in reputable journals. They're made in-house to ensure superior quality and efficiency. We offer custom services to meet all your needs. These antibodies are validated in Western Blotting, Immunohistochemistry, and ELISA. Boster can create custom antibodies for researchers all over the world.
The PPIG markers are a type II membrane proteins that bind to a specific molecule in cells. Boster Bio offers many benefits, including a troubleshooting and analysis guide. It is useful for both animal and plant research and helps researchers to determine the biological functions of a specific protein. Scientists must understand how this protein is expressed in the body.
This antibody is extremely specific and sensitive and reacts to human CD8a. It can either be stored at 4°C for a year or frozen when it is not in use. Boster Bio Anti-Human CD8a can be used with mice, rats, and humans. It is a monoclonal antibody with a high affinity for human CD8a. It stain about one million cells in 100 microliters.
Both fibronectins and PPIG are cell proteins with N–glycosylation sites and play a crucial role in cell to-cell adhesion. These proteins are often expressed during fibrosis. They may be novel therapeutic targets. Similar effects also occur on cell shape, and migration. These effects are governed by the fibronectin and PPIG markers, and are influenced by their concentrations.
The apex of FN release from burn wounds was determined at five, fifteen, and twenty-one days post-burn. The fifth day saw the greatest increase in FN release, while the second period occurred between 15 and 21 days. Electropherograms were obtained for different time points after burning to assess the extractability of FN. Although FN apex levels differed significantly by treatment, both PPIG and SSD delayed FN release, similar to the effect of NaCl.
Initial expression levels for both proteins were low in skin. In subsequent stages of development, fibronectin was discovered and tenascin B was discovered. In the MeLiM melanomas model, however, MMP-2 expression and fibronectin levels decreased slowly. The levels of tenascin C, fibronectin, and tenascin in the experimental group were higher than those in the control group. This may be due to the metastatic activity.
Different immunoassay techniques were used to detect the PPIG marker, and fibronectin. Fibronectin was reconstituted with 0.1 M HEPES buffer pH 7.4, 0.01M EDTA and Tween 20, along with Triton X100. Once the antibodies bound to the fibronectin molecules, the SPR signals changed in proportion to the amount of the protein. The immune complexes of antibodies were dissociated in a solution containing 0.01 M Glycine, pH 2.0.
PMID: 8973360 by Nestel F.P., et al. RS cyclophilins: identification of an NK-TR1-related cyclophilin.
PMID: 9153302 by Bourquin J.-P., et al. A serine/arginine-rich nuclear matrix cyclophilin interacts with the C-terminal domain of RNA polymerase II.