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616467

ZDON

≥98% (HPLC), powder, transglutaminase 2 inhibitor, Calbiochem®

Synonim(y):

Transglutaminase 2 Inhibitor, ZDON, Z-DON, 6-diazo-5-oxo-norleucine tetrapeptide, TG2 Inhibitor

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Rozmiar/SKUDostępnośćCena netto
5 mg

Dostępne do wysyłki DZISIAJzKuehne + Nagel Sp. z o.o.

1260,00 zł

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C31H45N7O9
Masa cząsteczkowa:
659.73
UNSPSC Code:
12352200
NACRES:
NA.54
Assay:
≥98% (HPLC)
Form:
powder
Storage condition:
OK to freeze

1260,00 zł


Dostępne do wysyłki DZISIAJSzczegóły


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Nazwa produktu

Transglutaminase 2 Inhibitor, ZDON, A cell-permeable, peptide-based, irreversible inhibitor of transglutaminase 2 (TG2; IC50 = 150 nM for recombinant TG2). Reacts with the active site cysteine of TG2.

Quality Segment

assay

≥98% (HPLC)

form

powder

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze

color

off-white

solubility

DMSO: 50 mg/mL

shipped in

ambient

storage temp.

−20°C

General description

A cell-permeable, peptide-based (Z- QVPL) irreversible inhibitor of transglutaminase 2 (TG2) (IC50 = 150 nM for recombinant TG2) that acts by reacting with the active site cysteine of TG2. Exhibits far less potency against TG1 and TG3. Shown to significantly increase PGC-1a and cytochrome c mRNA levels in Q7 and Q111 cells (~50 mM). Also shown to enhance cytochrome c promoter activity by 250% in Q111 cells. Exhibits protective effect in cells exposed to 3-nitropropionic acid and NMDA, however, it does not directly affect mitochondrial bioenergetics.

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Other Notes

McConoughey, S. J., et al. 2010. EMBO Mol. Medicine.2, 349.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)
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Ta pozycja
475992420144565851
description

A cell-permeable, peptide-based, irreversible inhibitor of transglutaminase 2 (TG2; IC50 = 150 nM for recombinant TG2). Reacts with the active site cysteine of TG2.

description

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description

The SHP1/2 PTPase Inhibitor, NSC-87877, also referenced under CAS 56932-43-5, controls the biological activity of SHP1/2 PTPase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

form

powder

form

powder

form

solid

form

solid

assay

≥98% (HPLC)

assay

≥99% (HPLC)

assay

≥95% (HPLC)

assay

≥97% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

2-8°C

storage condition

OK to freeze

storage condition

OK to freeze, protect from light

storage condition

protect from light, OK to freeze

storage condition

OK to freeze, desiccated (hygroscopic), protect from light


Klasa składowania

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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Questions

  1. Do you have any validations for Western blot showing that the provided ZDON lowers the TGM2 proteins levels? How have you validated TGM2 activity inhibition by ZDON if not by Western blot?

    1 answer
    1. 616467 Sigma-Aldrich Transglutaminase 2 Inhibitor, ZDON has not been validated in house in a Western Blotting application. It is a cell-permeable, peptide-based (Z- QVPL) irreversible inhibitor of transglutaminase 2 (TG2) (IC50 = 150 nM for recombinant TG2) that acts by reacting with the active site cysteine of TG2.
      This information is derived from the publication referenced on the MilliporeSigma website:
      McConoughey, S. J., et al. 2010. EMBO Mol. Medicine. 2, 349.

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