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| Protein Electrophoresis and Western> | Twenty-four hours post-transfection, 1. crude cell lysates were prepared and separated on gradient 4–20% SurePage gels (GenScript) for western blots using rabbit anti-GFP (#ab290, Abcam, dilution 1:1000), rabbit anti-NFKB1 (#13586, Cell Signaling, dilution 1:500) and rabbit anti-β-actin (#ab8227, Abcam, dilution 1:10000) antibodies; 2. cytoplasmic and nuclear fractions were prepared using NE-PER™ Nuclear and Cytoplasmic Extraction Reagents (Thermo Fisher Scientific) and separated on gradient 4-20% SurePage gels (GenScript) with antibodies specified above. | Get A Quote |
The molecular basis of increased hemoglobin in Andean Aymara highlanders is unknown. We conducted an integrative analysis of whole-genome-sequencing and granulocytes transcriptomics from Aymara and Europeans in Bolivia to explore genetic basis of the Aymara high hemoglobin. Differentially expressed and spliced genes in Aymaras were associated with inflammatory and hypoxia-related pathways. We identified transcripts with 4th or 5th exon skipping of NFKB1 (AS-NFKB1), key part of NF-kB complex, and their splicing quantitative trait loci; these were increased in Aymaras. AS-NFKB1 transcripts correlated with both transcripts and protein levels of inflammatory and HIF-regulated genes, including hemoglobin. While over... More