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Merck
모든 사진(1)

문서

65906

Sigma-Aldrich

Phalloidin–Atto 647N

BioReagent, suitable for fluorescence, ≥80% (HPLC)

동의어(들):

Atto 647N, Atto 647N-Phalloidin

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About This Item

UNSPSC 코드:
12171501
NACRES:
NA.32

제품 라인

BioReagent

분석

≥80% (HPLC)

제조업체/상표

ATTO-TEC GmbH

λ

in methanol

UV 흡수

λ: 640-646 nm Amax

적합성

suitable for fluorescence

검출 방법

fluorometric

저장 온도

−20°C

일반 설명

Phalloidin–Atto 647N is a new fluorescentlabel targeting the red spectral region. Atto 647N is a cationic dye, and postcoupling, it carries a net electrical charge of +1.Like most Atto labels, the absorption andfluorescence of Atto 647N are independent of pH between 2-11. Atto 647N issupplied in the form of a mixture containing two isomers having identicalfluorescence and absorption properties. Atto labels have rigid structures thatdo not show any cis-trans-isomerization.

애플리케이션

Phalloidin–Atto 647Nis designed to be used for labelling DNA, RNA, or proteins. Fluorescentconjugates of phalloidin are used to label actin filaments for histologicalapplications. Some structural features of phalloidin are required for thebinding to actin.

특징 및 장점

Characteristic features of the Phalloidin Atto488 are:
  1. StrongAbsorption.
  2. HighFluorescence quantum yield.
  3. HighPhotostability.
  4. MinimalTriplet formation.
  5. GoodSolubility.
  6. Excellent Ozone Resistance.

법적 정보

This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.

픽토그램

Skull and crossbones

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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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문서 라이브러리 방문

Dagmar A Brüggemann et al.
International journal of molecular sciences, 9(8), 1472-1488 (2009-03-28)
Muscle contraction studies often focus solely on myofibres and the proteins known to be involved in the processes of sarcomere shortening and cross-bridge cycling, but skeletal muscle also comprises a very elaborate ancillary network of capillaries, which not only play
Georgios Trichas et al.
BMC biology, 6, 40-40 (2008-09-17)
Transgenic animals are widely used in biomedical research and biotechnology. Multicistronic constructs, in which several proteins are encoded by a single messenger RNA, are commonly used in genetically engineered animals. This is currently done by using an internal ribosomal entry
Catherine Pfefferli et al.
Nature communications, 8, 15151-15151 (2017-05-04)
The existence of common mechanisms regulating organ regeneration is an intriguing concept. Here we report on a regulatory element that is transiently activated during heart and fin regeneration in zebrafish. This element contains a ctgfa upstream sequence, called careg, which
Inbar Schlachet et al.
ACS applied materials & interfaces, 11(24), 21360-21371 (2019-05-28)
Intranasal administration of nano-drug-delivery systems emerged as an appealing strategy to surpass the blood-brain barrier and thus increase drug bioavailability in the central nervous system. However, a systematic study of the effect of the structural properties of the nanoparticles on
Ceniz Zihni et al.
Nature cell biology, 19(9), 1049-1060 (2017-08-22)
Polarized epithelia develop distinct cell surface domains, with the apical membrane acquiring characteristic morphological features such as microvilli. Cell polarization is driven by polarity determinants including the evolutionarily conserved partitioning-defective (PAR) proteins that are separated into distinct cortical domains. PAR

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