The largest database of trusted experimental protocols

Atomlab 400

Manufactured by Mirion Technologies
Sourced in United States

The Atomlab 400 is a radiation detection and measurement device designed for use in laboratory settings. It is capable of accurately measuring radiation levels and provides essential data for radiation safety and analysis purposes.

Automatically generated - may contain errors

6 protocols using atomlab 400

1

FDG Radiochemical Synthesis Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
FDG was prepared through nucleophilic 18F-fluorination and hydrolysis of mannose triflate by the Stanford Cyclotron Radiochemistry Facility. 18F was made in a GE PETtrace cyclotron and the production was performed via cassette-based automated synthetic module (FASTlab, GE Healthcare). Quality control tests were performed according to USP823. The radiotracer was used within 8 h after production due to its short halftime (τ1/2 = 1.8 h). Radioactivity was measured using a dose calibrator (Atomlab 400, Biodex) prior to each experiment.
+ Open protocol
+ Expand
2

Radionuclide Labeling of Elastin-like Polypeptide

Check if the same lab product or an alternative is used in the 5 most similar protocols
An ELP with the sequence, (VPGVG)120(GY)7, was
recombinantly synthesized by overexpression of a synthetic gene encoding the ELP
in a pET-24a+ expression vector (Novagen Inc., Madison, Wi) in BLR(DE3)
competent E. coli (Edge BioSystems, Gaithersburg, MD) using
previously published methods [21 (link),
28 (link)]. A summary of the
molecular biology methods used for ELP genetic expression, synthesis, and
purification can be found in the Supplemental Materials.
Radionuclide labeling, for both 125I and 131I, was
performed using the iodogen oxidative reaction method [29 (link)]. Na125I and Na131I
were purchased from Perkin Elmer (Boston, MA) and reacted with 500 μM
ELP in Pierce® pre-coated IODOGEN tubes (Fisher Scientific, Hampton, NH)
on ice for 30 min. The product was purified by centrifugal ultrafiltration using
40K molecular weight cut off (MWCO) Zeba Spin Desalting Columns
(ThermoScientific, Rockford, IL) at 2500 rpm for 3 min at 4°C to remove
any unreacted radioiodine. The desired concentration of ELP was obtained by
mixing the reaction product with unlabeled ELP to bring the final concentration
of ELP to 1000 μM. Radioactivity was measured using the AtomLab 400 dose
calibrator (Biodex, Shirley, NY).
+ Open protocol
+ Expand
3

Automated [18F]FDG Radiopharmaceutical Production

Check if the same lab product or an alternative is used in the 5 most similar protocols
[18F]FDG was prepared through
nucleophilic 18F-fluorination and hydrolysis of mannose
triflate by the Stanford Cyclotron Radiochemistry Facility. 18F was made in a GE PETtrace cyclotron and the production was performed
via cassette-based automated synthetic module (FASTlab, GE Healthcare).
Quality control tests were performed according to USP823. The radiotracer
was used within 8 h after production due to its short halftime (τ1/2 = 1.8 h). Radioactivity was measured with a dose calibrator
(Atomlab 400, Biodex) prior to each experiment.
+ Open protocol
+ Expand
4

Single-Cell Radioactivity Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
An automatic gamma counter system (Hidex) was utilized to measure the radioactivity of individual cells. Single radiolabeled cells were transferred to 250 μl microcentrifuge tubes and loaded into racks for automated gamma counting. Each tube contained 100 μl fresh media and 1 μl droplet from the single-cell dispenser (composed of 99.7% PBS sheath fluid, 0.3% cell culture media solution). As a result, the radioactivity in each tube mainly originated from the single cell as the efflux in the cell solution was highly diluted. The radioactivity values in counts per second were converted to Bq through a calibration curve constructed from the measurement of serially diluted FDG solutions and a standard dose calibrator (Biodex, Atomlab 400). To confirm the singularity of dispensed single cells, we divided the solution in each tube equally into two or three vials and measured the activity of each fraction by gamma counting and PET imaging. The rationale for this experiment is that the contents of the single cell cannot be fractionated into multiple vials.
+ Open protocol
+ Expand
5

Iodine-131 Labeling of Elastin-like Polypeptides

Check if the same lab product or an alternative is used in the 5 most similar protocols
Conjugation of 131Iodine was carried out using the Iodogen method for the direct oxidation of tyrosine peptides97 (link). Briefly, Na131I was purchased from Perkin Elmer and reacted with 500 μM ELP in Pierce® IODOGEN pre-coated tubes (Thermo Fisher Scientific) on ice for 30 min29 (link). Each ELP molecule contains 7 tyrosine subunits to provide abundant sites for radiolabeling. Unreacted iodine was removed from the mixture using Zeba Spin Desalting Columns, 40K MWCO (Thermo Fisher Scientific). Next, the solution was centrifuged at 1000 rcf for 4 min at 4°C. Radioactivity levels were verified using the AtomLab 400 dose calibrator (Biodex). The 131I-ELP conjugate was then mixed with unreacted ELP to bring the final ELP concentration to 1000 μM and the radioactivity to its desired level. For all radioactivity concentrations, tyrosine iodination accounted for less than 10% of total tyrosine content in the ELP depots.
+ Open protocol
+ Expand
6

Siemens Inveon PET Platform Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols
The Siemens Inveon PET platform was used to perform imaging experiments. Its detector consists of lutetium oxyorthosilicate (LSO) crystals coupled through a light-guide to position sensitive photo-multiplier tubes. The LSO crystals are arranged in 16 detector blocks, each with 4 detectors axially which are divided into 20 × 20 crystal arrays. The ring diameter is 16.1 cm and the axial length 12.7 cm, with individual crystal sizes of 1.5 × 1.5 × 10 mm3. For the acquisitions, an energy window of 350–650 keV and a coincidence timing window of 3.432 μs were used.
Prior to injection into the phantoms, the radionuclide activity was measured in an Atomlab 400 dose calibrator (Biodex Medical Systems, NY, USA). Emission data was acquired in list mode, and the Inveon Acquisition Workplace (v. 1.5.0.28) was used to bin the data into sinograms and reconstruct the images. Images were reconstructed with three image reconstruction procedures available, using the default parameters. The reconstruction procedures were 2D FBP (Fourier rebinning, Nyquist cut-off 0.5), OSEM3D-MAP (2 OSEM3D iterations, 18 MAP iterations, 1.5-mm requested resolution), and OSEM2D (4 iterations).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!