Sentence examples for 1 lds from inspiring English sources

This view changed when it was realized that 1) LDs are present in essentially all cell types, including those for which mere energy storage does not seem to be the main purpose; 2) LDs, particularly in nonadipose tissues, undergo very dynamic changes of formation and degradation; and 3) LDs represent a reservoir of bioactive lipids and lipid-derived hormones in adipose and nonadipose tissues.

We simulated regions with 1 LD block (6 SNPs), 2 LD blocks (10 SNPs), 6 LD blocks (30 SNPs) or 24 LD blocks (120 SNPs).

We simulated 4 different LD patterns, in which a region may have 1 LD block (including 6 SNPs), 2 LD blocks (including 10 SNPs), 6 LD blocks (including 30 SNPs) and 24 LD blocks (including 120 SNPs), respectively, 40,000 replicates for each scenario.

One SNP rs17387019 was reported to be in perfect (r = 1) LD with rs61764370.

Beads were re-suspended in 1× LDS buffer with 10% BME and 1% NEM and incubated for 5 min at 95°C.

After binding, beads were washed five times with 1 mL of PBST and heated at 70°C in 20 µL of 1× LDS loading buffer (Invitrogen) for 10 minutes.

Proteins were re-solubilized in 25 μl 1× LDS NuPAGE loading buffer and incubated for 10 minutes at 70°C.

Immunoprecipitates were eluted by boiling in 1× LDS loading buffer (Invitrogen) and separated by LDS-PAGE (Invitrogen).

Cells were washed with PBS and lysed with 1× LDS sample buffer and 1× sample reducing agent (Life Technologies).

Reactions were stopped at the time shown and incubated at 95°C in 1× LDS (Invitrogen) 5 mM DTT for 1 min.

The lysates were incubated for 2 h rotating at 4°C, after which they were washed 3 times with Saito's modified lysis buffer, eluted by boiling 10 min in 40 μl 1× LDS buffer (Life Technologies).