Produkto kodas: N/A
Avaibility : Liko
Product Name Amatoxin, Recombinant Protein
Full Product Name Recombinant Amanita phalloides Amatoxin
Product Synonym Names Recombinant Amatoxin; Amatoxin; Alpha-amanitin Gamma-amanitin
Research Use Only For Research Use Only. Not for use in diagnostic procedures.
Sequence Positions 1-8aa; Cytoplasmic domain
3D Structure ModBase 3D Structure for P85421
Host E Coli or Yeast or Baculovirus or Mammalian Cell
Purity/Purification >=90% (lot specific)
Form/Format Liquid containing glycerol
Tag Information This protein contains an N-terminal tag and may also contain a C-terminal tag. Tag types are determined by various factors including tag-protein stability, please inquire for tag information.
Sterility Sterile filter available upon request.
Endotoxin Low endotoxin available upon request.
Species Amanita phalloides (Death cap)
Preparation and Storage Store at -20 degree C. For extended storage, store at -20 or -80 degree C.
ISO Certification Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes Small volumes of Amatoxin recombinant protein vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
NCBI GI # 205686182
NCBI Accession # P85421.1

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Amatoxin is the aggregate name of a subgroup of in any event nine related harmful mixtures found in three genera of toxic mushrooms (Amanita, Galerina and Lepiota) and one animal categories (Conocybe filaris) of the class Conocybe. From the amanita, the most quite is the passing cap (Amanita phalloides). Amatoxins are deadly in even little dosages, as little as a large portion of a mushroom. In contrast to many ingested harms, they can’t be obliterated by heat without annihilating the mushrooms past edibility first, so cooking the toxic mushrooms doesn’t lessen their lethality.

Side effects of openness

Upon openness to amatoxins, the liver is the main organ influenced as it is the organ which is first experienced after ingestion in the gastrointestinal lot. There is no proof that amatoxins are assimilated through skin. One examination done on mice shows that alpha-Amanitin isn’t assimilated through skin and consequently can not have any harmful impacts. All the more explicitly, openness to amatoxins may cause bothering of the respiratory plot, migraine, discombobulation, sickness, windedness, hacking, a sleeping disorder, the runs, gastrointestinal unsettling influences, back torment, urinary recurrence, liver and kidney harm, or demise whenever ingested or breathed in. For instance, if β-amanitin interacts with skin, it might cause aggravation, consumes, redness, extreme agony, and could be assimilated through the skin, making comparable impacts openness by means of inward breath and ingestion. Contact with the eyes may bring about bothering, corneal consumes, and eye harm. People with previous skin, eye, or focal sensory systems issues, weakened liver, kidney, or aspiratory capacity might be more powerless with the impacts of this substance.

Amatoxin harming shows a biphasic clinical example. An underlying (12–24 hours) time of intense side effects is trailed by a time of relative wellbeing that goes on for 12–24 hours. After this period, liver and kidney disappointment happen with death commonly happening from day 2 onwards.

The assessed least deadly portion is 0.1 mg/kg or 7 mg of poison in grown-ups. Their quick intestinal ingestion combined with their thermostability prompts fast improvement of poisonous impacts in a moderately brief timeframe. The most extreme impacts are harmful hepatitis with centrolobular rot and hepatic steatosis, just as intense tubulointerstitial nephropathy, which inside and out prompt serious liver disappointment and kidney disappointment.


There are numerous episodic and incompletely contemplated medicines being used around the world. One investigation in mice showed invalid outcomes for every considered treatment. Medicines showing no discernable worth included N-acetylcysteine, benzylpenicillin, cimetidine, thioctic corrosive, and silybin.

Treatment includes high-portion penicillin just as strong consideration in instances of hepatic and renal injury. Silibinin, an item found in milk thorn, is a possible counteractant to amatoxin harming, albeit more information should be gathered. Careful consideration is given to keeping up hemodynamic solidness, despite the fact that if hepatorenal disorder has built up the visualization is watched, best case scenario.


Presence of amatoxins in mushroom tests might be recognized by the Meixner test (otherwise called the Wieland test). The amatoxins might be quantitated in plasma or pee utilizing chromatographic procedures to affirm a determination of harming in hospitalized patients and in after death tissues to help in a medicolegal examination of a presumed deadly overdosage.

In 2020, a monoclonal counter acting agent based parallel stream immunoassay has been built up that can rapidly and specifically identify amatoxins.This test delicately recognizes alpha-amanitin and gamma-amanitin (obviously identifies 10 ng/mL), and shows marginally less recognition for beta-amanitin (0.5% cross-reactivity; 2000 ng/mL). Albeit this test cross-responds with phallotoxins at 0.005% (200,000 ng/mL), the phallotoxins would not meddle in pee examining and there are exceptionally uncommon occasions where a mushroom produces phallotoxins without delivering amatoxins.

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