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Female pupae from each temperature were split into three experimental groups: non-injected, injected with control solution, and injected with hormone solution (see below).
One hundred kilograms of 56 μm-diameter mZVI (~ 70 g L− 1) was suspended in 1.5 m3 of guar gum (~ 7 g L− 1) solution and injected into the test area.
The organic (top) phase was washed with a sodium hydroxyl solution and injected in a gas chomatograph (GC).
Two milligrams of RITC-labeled nanoparticles (GS-PEG, GS-PEG-Apt, and GS-PEG/HA2-Apt) were dispersed in 100 μL physiological saline solution and injected into the tail vein.
They were concentrated in Hanks' buffered salt solution and injected into the frontal part of the right and left hemisphere (200.000 cells/injection in a total volume of 2 µl).
Each vaccine dose was a lyophilized mixture of the four lipopeptides that was reconstituted with 0.5 ml of a 5% isotonic glucose solution and injected either intradermally (0.1 ml, 100 µg of each peptide) or intramuscularly (0.5 ml, 500 µg of each peptide).
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This "delivery by feeding" is just as effective at inducing gene silencing as more costly and time-consuming delivery methods, such as soaking the worms in dsRNA solution and injecting dsRNA into the gonads.
25 Quality of artesunate samples was determined by dissolving the tablet in methanol to produce a 2.5 mg/mL solution and injecting it onto the HPLC column.
Therapeutic agents can be easily mixed with the free flowing polymer solutions and injected into the subcutaneous tissue or target site that could form a viscoelastic gel and act as therapeutic agents release depot.
The sorted cells (7.5×104 or 5×104 cells/recipient) were resuspended in 30 µl each of Hanks' balanced salt solutions and injected into the footpad of naive mice.
Stealth RNAi (MSS207677, MSS207678) designed specifically against aPKCι/λ and stealth RNAi negative control were purchased from Invitrogen, resuspended with DEPC water to prepare 20 µM stock solutions, and injected at a final concentration of 8 µM.
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