? BMBI CORE The Biochemistry and Molecular Biology Instrumentation (BMBI) module is an essential core resource that continues to be heavily used by the majority of our investigators to support the preparation and analysis of biological samples. The BMBI core module resources consist of common instrumentations such as autoclaves, various spectrophotometers, centrifuges, incubators, microplate readers, immunoassay protein analyzers, polymerase chain reaction (PCR) machines for DNA and RNA analysis. While most of these instruments are basic, their utilization is extensive and critically important for the progress of research programs in each laboratory. The majority of our core investigators employ basic biochemistry and molecular biological approaches to prepare and analyze quantitatively and qualitatively various biological samples. These include RNA, DNA, and protein samples obtained directly from tissue specimens or extracted from heterologous cell- and non-cell-based protein expressing systems. Besides the common instruments, this module has available specialized spectrometers for detailed protein structural and functional analysis, including fluorescence, UV-visible absorbance, Fourier transform infra-red, and customized circular dichroism (CD) spectroscopies. In addition, sophisticated multi-angle and quasi-elastic light scattering instruments are available. Our core investigators can determine gene expression profiles using high throughput microfluidic assays, a next generation single cell RNA-sequencing (scRNA-seq) PCR approach. A recently purchased automated Western immunoblot system allows for quantification of low abundant proteins via a sensitive immunoassay reaction involving minimal sample manipulation with data being analyzed digitally. Our newly acquired Molecular Devise SpectraMax iD3 microplate reader permits quantification at multiplex formats (6 to 384-well) for absorbance, fluorescence, and luminescence, thus enabling multiple biochemical assays at the same time. The BMBI module infrastructure and instrumentation capabilities are quintessential for our investigators day-to-day scientific productivity by stimulating interactions among our researchers and facilitating the quick integration of new recruits.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
2P30EY000331-53
Application #
10020830
Study Section
Special Emphasis Panel (ZEY1)
Project Start
1997-03-01
Project End
2025-06-30
Budget Start
2020-08-01
Budget End
2021-07-31
Support Year
53
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Glasgow, Ben J; Abduragimov, Adil R (2018) Interaction of ceramides and tear lipocalin. Biochim Biophys Acta Mol Cell Biol Lipids 1863:399-408
Demer, Joseph L (2018) Knobby Eye Syndrome. Strabismus 26:33-41
Glasgow, Ben J; Abduragimov, Adil R (2018) Ligand binding studies by high speed centrifugal precipitation and linear spectral summation using ultraviolet-visible absorption spectroscopy. MethodsX 5:345-351
Hazim, Roni A; Volland, Stefanie; Yen, Alice et al. (2018) Rapid differentiation of the human RPE cell line, ARPE-19, induced by nicotinamide. Exp Eye Res 179:18-24
Glasgow, Ben J; Abduragimov, Adil R (2018) Data on Orphan tear lipid analogs, synthesis and binding to tear lipocalin. Data Brief 18:999-1004
Sarria, Ignacio; Cao, Yan; Wang, Yuchen et al. (2018) LRIT1 Modulates Adaptive Changes in Synaptic Communication of Cone Photoreceptors. Cell Rep 22:3562-3573
Peng, Yingqian; Baulier, Edouard; Ke, Yifeng et al. (2018) Human embryonic stem cells extracellular vesicles and their effects on immortalized human retinal Müller cells. PLoS One 13:e0194004
Clark, Robert A; Demer, Joseph L (2018) The Globe's Eccentric Rotational Axis: Why Medial Rectus Surgery Is More Potent than Lateral Rectus Surgery. Ophthalmology 125:1234-1238
Van Eps, Ned; Altenbach, Christian; Caro, Lydia N et al. (2018) Gi- and Gs-coupled GPCRs show different modes of G-protein binding. Proc Natl Acad Sci U S A 115:2383-2388
Shin, Andrew; Park, Joseph; Demer, Joseph L (2018) Opto-mechanical characterization of sclera by polarization sensitive optical coherence tomography. J Biomech 72:173-179

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