Reconstitution Buffer 4 (BSA/HCl)
Reconstitution Buffer 4 (BSA/HCl) Summary
Specifications
Product Datasheets
Citations for Reconstitution Buffer 4 (BSA/HCl)
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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TGF-beta signaling and Creb5 cooperatively regulate Fgf18 to control pharyngeal muscle development
Authors: J Feng, X Han, Y Yuan, CK Cho, E Jane?ková, T Guo, S Pareek, MS Rahman, B Zheng, J Bi, J Jing, M Zhang, J Xu, TV Ho, Y Chai
Elife, 2022-12-21;11(0):. 2022-12-21
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TGFbeta2-Hepcidin Feed-Forward Loop in the Trabecular Meshwork Implicates Iron in Glaucomatous Pathology
Authors: A Ashok, S Chaudhary, AE Kritikos, MH Kang, D McDonald, DJ Rhee, N Singh
Invest. Ophthalmol. Vis. Sci., 2020-03-09;61(3):24. 2020-03-09
FAQs
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Are the Reconstitution Buffers, Catalog #s RB01-RB07, sterile?
The Reconstitution Buffers, Catalog #s RB01 through RB07, are RUO (Research Use Only) products and are not guaranteed to be sterile. As part of Quality Control process prior to release, Reconstitution Buffers RB01 through RB07 undergo testing including a 7 day microbial Bioburden test, as well as a test for Endotoxin via LAL method (specification of < 0.25 EU/mL). If sterile buffer is required, it is recommended the buffer can be filtered through a 0.2 micron filter designed for use with biological fluids
Reviews for Reconstitution Buffer 4 (BSA/HCl)
Average Rating: 4.5 (Based on 4 Reviews)
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I reconstituted the BMP-10 protein using this buffer and it was very convenient and saved time since I did not need to measure out the reagents myself. In addition, I feel my future experiments will be more consistent knowing that my protein is prepared the same way each time.
Image caption: 20x magnification of marmoset embryonic stem cells, grown in media supplemented with human nodal protein that was reconstituted with this buffer #RB04. cells had normal morphology and didn't have spontaneous differentiation., there were no obvious cytotoxic effects from the 4mM HCl present in this buffer.
Needed this because we had no HCl in the lab, needed to reconstitute 'Recombinant Human Nodal Protein'. this saved me alot of time not having to order HCl, and make a small amount of this buffer that wouldn't be used for anything else. served its purpose in becoming a crucial component for my marmoset cell culture media.
