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94072

Phalloidin–Atto 565

suitable for fluorescence, ≥80.0% (HPLC)

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Velikost baleníSkladová položkaDostupnostCena
10 nmol
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12 500,00 Kč

O této položce

NACRES:
NA.32
UNSPSC Code:
12352108

12 500,00 Kč


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Quality Segment

assay

≥80.0% (HPLC)

form

solid

mol wt

Mw 1394 g/mol

manufacturer/tradename

ATTO-TEC GmbH

λ

in methanol

UV absorption

λ: 562.0-568.0 nm Amax

suitability

suitable for fluorescence

storage temp.

−20°C

General description

Atto 565 is a novel fluorescent label that belongs to the class of Rhodamine dyes. It shows a strong absorption, high fluorescence quantum yield, high thermal and photostability, and a very little triplet formation. Atto 565 consists of a mixture of two isomers with practically identical optical absorption and emission Phalloidin is a fungal toxin isolated from the poisonous mushroom Amanita phalloides. Its toxicity is attributed to the ability to bind F actin in liver and muscle cells. As a result of binding phalloidin, actin filaments become strongly stabilized. Phalloidin has been found to bind only to polymeric and oligomeric forms of actin, and not to monomeric actin. The dissociation constant of the actin-phalloidin complex has been determined to be on the order of 3 x 10-8. Phalloidin differs from amanitin in rapidity of action; at high dose levels, death of mice or rats occurs within 1 or 2 hours. Fluorescent conjugates of phalloidin are used to label actin filaments for histological applications. Some structural features of phalloidin are required for the binding to actin. However, the side chain of amino acid 7 (g-d-dihydroxyleucine) is accessible for chemical modifications without appreciable loss of affinity for actin.

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Tato položka
930420449768825
suitability

suitable for fluorescence

suitability

suitable for fluorescence

suitability

suitable for fluorescence

suitability

suitable for fluorescence

form

solid

form

solid

form

-

form

solid

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

assay

≥80.0% (HPLC)

assay

≥90%

assay

≥90% (HPLC)

assay

≥90% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

UV absorption

λ: 562.0-568.0 nm Amax

UV absorption

-

UV absorption

-

UV absorption

λ: 629-635 nm Amax


Skladovací třída

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Osvědčení o analýze (COA)

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Sortimentní položky

Barviva Atto jsou řadou fluorescenčních barviv, která splňují kritické potřeby moderních fluorescenčních technologií.

Atto dyes are a series of fluorescent dyes that meet the critical needs of modern fluorescent technologies.


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We previously developed a 14-day culture protocol under potentially GMP, chemically defined conditions, to generate chondroprogenitors from human embryonic stem cells (hESCs). In vivo work has confirmed the cartilage repair capacity of these cells in a nude rat osteochondral defect
Thomas Bise et al.
Scientific reports, 10(1), 11551-11551 (2020-07-16)
Zebrafish can regenerate their damaged hearts throughout their lifespan. It is, however, unknown, whether regeneration remains effective when challenged with successive cycles of cardiac damage in the same animals. Here, we assessed ventricular restoration after two, three and six cryoinjuries
Mariangela Sabatella et al.
Cell reports, 34(2), 108608-108608 (2021-01-14)
Hereditary DNA repair defects affect tissues differently, suggesting that in vivo cells respond differently to DNA damage. Knowledge of the DNA damage response, however, is largely based on in vitro and cell culture studies, and it is currently unclear whether DNA repair



Globální číslo obchodní položky

Skladová položkaGTIN
SML0254-50MG04061832260877
SML0254-10MG04061833222324
94072-10NMOL04061837737664

Questions

  1. Currently working with PEEK (Poly Ether Ether Ketone) and its been fixed stained cells on the surface. The F-Actin phalloidin TRIT-C I used might have interacted with the polymer. Does the product Phalloidin Atto 565 and product number 94072 would do the same?

    1 answer
    1. PEEK is considered a high-performance polymer but is not typically used in staining applications due to its high cost. In typical staining applications, glass or less expensive plastics are utilized. There is no available information on why the F-ctalin phalloidin labeled with TRITC would interact with PEEK, nor is there information on whether switching to an ATTO 565 would eliminate the problem related to the interaction of the PEEK for the same application.

      Another consideration might be whether a coating was applied to the PEEK. There have been cases in the past where a particular coating would provide a high background when viewed under either a light or fluorescent microscope. Glass slides and plastics are sometimes coated with a substance that provides a positive charge to the slide. If cells and the solid substrate both have a negative charge, the tissue will not remain attached to the solid surface during staining. While a light coating is typically applied, if the amount of coating is too thick, it could cause a high background on the slides when viewed with either a light or fluorescent microscope. It is advisable to check the PEEK surface with no tissue or cells attached, as a complaint on a high background observed in the past was originally thought to be due to the coating on the slide but turned out to be from the slides themselves.

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