Titlebook: Hypoxia; Methods and Protocol L. Eric Huang Book 2018 Springer Science+Business Media, LLC 2018 ChIP.CRISPR.Cas9 Gene Editing.VHL binding.R

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https://doi.org/10.1007/978-3-663-01633-5s in an increase of red blood cell (RBC) production and delivery of more oxygen to tissues. Upon rapid return to normoxia, hypoxia-induced polycythemia is overcorrected by neocytolysis, a transient destruction of preferentially young RBCs bearing low catalase (downregulated by hypoxia-stimulated mic

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https://doi.org/10.1007/978-3-663-05587-7hod to induce hypoxia in zebrafish embryos and larvae. This protocol is easy and reproducible and does not require expensive equipment or specialized devices. It can be adapted in large, medium, and small scales. This protocol is also well-suited for experiments requiring chemical drug treatment and

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Kinetic Analysis of HIF Prolyl Hydroxylases,tion rate, and inhibitory properties of the isoenzymes in vitro. Here we describe an assay measuring the substrate hydroxylation-coupled decarboxylation of radioactive 2-oxoglutarate to radioactive carbon dioxide as a fast, efficient, and diverse method to analyze the enzyme kinetics of HIF-P4Hs.

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Mass Spectrometry and Bioinformatic Analysis of Hydroxylation-Dependent Protein-Protein Interactionulated in an intracellular signaling network. Protein hydroxylation, which is a posttranslational modification catalyzed by oxygen-dependent enzymes, is a crucial regulator of protein-protein interactions. Under low oxygen conditions, the activity of many hydroxylases is inhibited, which results in

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Acquisition of Temporal HIF Transcriptional Activity Using a Secreted Luciferase Assay,ition of dynamic and high-throughput data on HIF transcriptional activity during hypoxia and pharmacological activation of HIF. The sensitivity of the assay allows for the secreted luciferase to be consecutively sampled (as little as 1% of the total supernatant) over an extended time period, thus al

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Fluorescence Lifetime Imaging Microscopy (FLIM) as a Tool to Investigate Hypoxia-Induced Protein-Prr fluorophore in close proximity to an appropriate acceptor fluorophore transfers emission energy to the acceptor, resulting in a shorter lifetime of the donor fluorescence. When the respective FRET donor and acceptor are fused with two proteins of interest, a reduction in donor lifetime, as detecte

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Transcriptional Profiling Using RNA-Seq to Study Hypoxia-Mediated Gene Regulation,he transcription factors known as hypoxia-inducible factors (HIFs). HIF1, a heterodimer of hypoxia-stabilized subunit HIF-1alpha and a constitutively expressed subunit HIF-1beta, serves as a key transcription factor that regulates gene expressions which are involved in cell growth, metabolism, and p

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Titlebook: Hypoxia; Methods and Protocol L. Eric Huang Book 2018 Springer Science+Business Media, LLC 2018 ChIP.CRISPR.Cas9 Gene Editing.VHL binding.R

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