제품 이름
HEPES solution, BioPerformance Certified, 1 M, suitable for cell culture, 0.2 μm filtered
grade
BioPerformance Certified
Quality Level
sterility
0.2 μm filtered
form
liquid
concentration
1 M
technique(s)
cell culture | mammalian: suitable
impurities
Bioburden, tested, DNase, RNase, Protease, Nickase, free, endotoxin, tested
pH
5.0-6.0
useful pH range
6.8-8.2
cation traces
Fe: <5 ppm, heavy metals (as Pb): <5 ppm
suitability
suitable for molecular biology
application(s)
diagnostic assay manufacturing
SMILES string
OCCN1CCN(CCS(=O)(O)=O)CC1
InChI
1S/C8H18N2O4S/c11-7-5-9-1-3-10(4-2-9)6-8-15(12,13)14/h11H,1-8H2,(H,12,13,14)
InChI key
JKMHFZQWWAIEOD-UHFFFAOYSA-N
General description
HEPES has been described as one of the best all-purpose buffers available for biological research. At biological pH, the molecule is zwitterionic, and is effective as a buffer at pH 6.8 to 8.2. HEPES has been used in a wide variety of applications, including tissue culture. It is commonly used to buffer cell culture media in air. HEPES finds its usage in in vitro experiments on Mg.
Application
RNAse HEPES has been used:
- To supplement Dulbecco′smodified Eagle′smedium for maintenance of cell line and RPMI medium to wash rat islets
- To recover purified ribonucleotide
- As a component of HEPES/KOH buffer and adenylation buffer for small RNA isolation and sequencing
- As a component in buffers used for nuclear extract preparation and also to supplement RPMI-1640 medium for maintenance of islets
저장 등급
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
문서
Human pancreatic cancer organoid biobank (PDAC organoids) with various KRAS mutations to aide in 3D cell culture and cancer research applications.
Expression of an uncleavable N-terminal RasGAP fragment in insulin-secreting cells increases their resistance toward apoptotic stimuli without affecting their glucose-induced insulin secretion.
Yang JY, et al.
The Journal of Biological Chemistry, 280(38), 32835-32842 (2005)
Timing of CRISPR/Cas9-related mRNA microinjection after activation as an important factor affecting genome editing efficiency in porcine oocytes.
Sato M, et al.
Theriogenology, 108, 29-38 (2018)
A Small RNA Isolation and Sequencing Protocol and Its Application to Assay CRISPR RNA Biogenesis in Bacteria.
Silas S, et al.
Bio-protocol, 8(4) (2018)
국제 무역 품목 번호
| SKU | GTIN |
|---|---|
| H3537-100ML | 04061833793435 |
| H3537-1L | 04061835545476 |
| H3537-500ML | 04061833793442 |