추천 제품
material
polyethersulfone
polypropylene
silicone seal
Quality Level
특징
holdup volume 175 mL
제조업체/상표
Viresolve®
파라미터
≤16 mL/min air diffusion at 3.45 bar (50 psig) and 23 °C (in water)
3.4 bar max. differential pressure (50 psid) at 25 °C (Reverse)
5.5 bar max. differential pressure (80 psid) at 25 °C (Forward)
600-1200 L process volume
기술
protein purification: suitable
카트리지 공칭 길이
10 in. (25 cm)
여과 면적
0.43 m2
불순물
≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
중량 추출물
≤35 mg/cartridge
기질
Viresolve® NFR
카트리지 코드
Code 7
일반 설명
Device Configuration: Cartridge
애플리케이션
Retrovirus removal
포장
Double Easy-Open bag
기타 정보
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Directions for Use
- Organism Retention: Retrovirus
- Mode of Action: Filtration (size exclusion)
- Application: Protein purification
- Intended Use: Viral clearance
- Instructions for Use: Please see the user guide (pg. 3) shipped with this product
- Storage Statement: Store at room temperature
- Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.
제조 메모
Sterilization Method
After wetting, may be autoclaved for 3 cycles of up to 60 min at 125 °C,
using liquid cycle, slow exhaust.
After wetting, may be autoclaved for 3 cycles of up to 60 min at 125 °C,
using liquid cycle, slow exhaust.
This product was manufactured with a Viresolve® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
분석 메모
Gravimetric Extractables: after a 10 minute 1.5 LPM/ft² flush and 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4 L
법적 정보
VIRESOLVE is a registered trademark of Merck KGaA, Darmstadt, Germany
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.
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