추천 제품
형태
gelatinous solid
Quality Level
포장
vial of 75 mg Sequa-brene (5 mg NaCl added)
저장 온도
2-8°C
InChI
1S/C10H24N2.C3H6Br2/c1-11(2)9-7-5-6-8-10-12(3)4;4-2-1-3-5/h5-10H2,1-4H3;1-3H2
InChI key
KZKAYEGOIJEWQB-UHFFFAOYSA-N
애플리케이션
Used as a protein/peptide carrier for protein sequencing.
재구성
See data sheet for preparation.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
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
Hewan A Belete et al.
PloS one, 6(11), e27469-e27469 (2011-11-17)
Cell wounding is an important driver of the innate immune response of ventilator-injured lungs. We had previously shown that the majority of wounded alveolus resident cells repair and survive deformation induced insults. This is important insofar as wounded and repaired
Samantha J Stehbens et al.
Nature cell biology, 16(6), 561-573 (2014-05-27)
Turnover of integrin-based focal adhesions (FAs) with the extracellular matrix (ECM) is essential for coordinated cell movement. In collectively migrating human keratinocytes, FAs assemble near the leading edge, grow and mature as a result of contractile forces and disassemble underneath
[Chemiluminescence of peritoneal macrophages activated by non-natural polyelectrolytes].
L G Korkina et al.
Doklady Akademii nauk SSSR, 282(1), 206-209 (1985-05-01)
L Bonsignore et al.
Leukemia, 31(3), 614-624 (2016-08-20)
Primary effusion lymphoma (PEL) is an incurable malignancy that develops in immunodeficient patients as a consequence of latent infection of B-cells with Kaposi's sarcoma-associated herpes virus (KSHV). Malignant growth of KSHV-infected B cells requires the activity of the transcription factor
Nicolas Christoforou et al.
Scientific reports, 7, 40285-40285 (2017-01-11)
Transdifferentiation has been described as a novel method for converting human fibroblasts into induced cardiomyocyte-like cells. Such an approach can produce differentiated cells to study physiology or pathophysiology, examine drug interactions or toxicities, and engineer cardiac tissues. Here we describe
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