추천 제품
Grade
BioPerformance Certified
Quality Level
분석
≥99.5% (titration)
형태
crystalline powder
저장 조건
dry at room temperature
기술
cell culture | mammalian: suitable
competitive inhibition ELISA: suitable
불순물
endotoxin and total aerobic microbial count, tested
색상
white
유용한 pH 범위
6.8-8.2
pKa(25 °C)
7.5
양이온 미량물
Fe: ≤5 ppm
흡수
≤0.05 at 260 in H2O at 0.1 M
≤0.05 at 280 in H2O at 0.1 M
적합성
suitable for Western blot
suitable for component for culture media
응용 분야
clinical research
diagnostic assay manufacturing
general analytical
life science and biopharma
외래 활성
DNase, RNase, NICKase, protease, none detected
SMILES string
OCCN1CCN(CC1)CCS(O)(=O)=O
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
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
HEPES also proves advantageous in various biological and biochemical processes. Its ampholytic nature makes it suitable as a separator for creating pH gradients in isoelectric focusing, a technique often employed in protein separation and analysis. Moreover, HEPES exhibits minimal interference with DNA-restriction enzyme reactions compared to buffers with fewer substituted amine groups, such as Tris. This makes it a preferred choice for applications involving DNA manipulation and analysis. Beyond these specific applications, HEPES is valuable in numerous other biological and biochemical processes, including immunoprecipitation, cell lysis, and live cell imaging. Its versatility, coupled with exceptional pH buffering capacity and minimal interaction with other molecules, establishes HEPES as an indispensable tool across diverse research domains.
애플리케이션
- To supplement Dulbecco′s modified Eagle′s medium to culture and maintain cell lines
- As a component of platelet suspension buffer
- To supplement Hank′s basic salt solution, which is used to wash pancreatic tissue
- As a component of wash buffer and blocking buffer in the purification and quantification of protein with enzyme-linked immunosorbent (ELISA) assay
- For the adjustment and maintenance of pH of biological solutions
- As a component of Hank′s balanced salt solution (HBSS) and dissociation medium to study neuronal development
- For homogenization of tissue and in the preparation of cytosolic and nuclear extract from cells
- As a component of keratinocyte and fibroblast culture medium
특징 및 장점
- Tested to confirm low levels of heavy metal contamination, ensuring suitability for various applications
- Highly soluble in water with a useful pH range of 6.8 - 8.2 and pKa of 7.5 at 25 °C
- Negligible metal ion binding
- Less toxic to cells than other buffers such as Tris and phosphate
- Stable in a wide pH range
- Tested for Endotoxins and Total Aerobic Microbial Count
- Free from DNase, NICKase, RNase, Endonuclease, Exonuclease and Protease
기타 정보
또한 이 제품과 함께 일반적으로 구입
호환 제품
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
프로토콜
This protocol describes a method for chemical cross-linking of proteins using formaldehyde. With the exception of zero-length cross-linkers, formaldehyde has the shortest cross-linking span (~2-3 Å) of any cross-linking reagent, thus making it an ideal tool for detecting specific protein-protein interactions with great confidence.
cAMP measurements are obtained using an ELISA assay (Harlow and Lane 1988). Commercial radio-immunoassays, or ELISA kits, to assay cAMP can be purchased from various manufacturers.
To determine the molecular weights of protein antigens, to study protein/protein interactions, to determine specific enzymatic activity, to monitor protein post-translational modifications and to determine the presence and quantity of proteins.
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.