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233483

Sigma-Aldrich

Coagulation Factor XIa, Human Plasma

Coagulation Factor XIa, Human Plasma, is a native coagulation factor XIa prepared from homogeneous Factor XI by activation with human Factor XIIa. Factor XIIa is removed after activation.

Synonyme(s) :

Coagulation Factor

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1 G
CA$480.00

CA$480.00


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1 G
CA$480.00

About This Item

Code UNSPSC :
12352202
Nomenclature NACRES :
NA.25

CA$480.00


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Niveau de qualité

Forme

liquid

Fabricant/nom de marque

Calbiochem®

Conditions de stockage

OK to freeze
avoid repeated freeze/thaw cycles

Conditions d'expédition

wet ice

Température de stockage

−70°C

Description générale

Native coagulation factor XIa from human plasma prepared from homogeneous Factor XI by activation with human Factor XIIa. Factor XIIa is removed after activation. In vivo, Factor XI is activated to Factor XIa via Factor XIIa and High Molecular Weight Kininogen (Cat. No. 422686). Factor XIa activates Factor IX to Factor IXa in a reaction that does not require membrane surfaces.

Conditionnement

Please refer to vial label for lot-specific concentration.

Avertissement

Toxicity: Standard Handling (A)

Forme physique

In 150 mM NaCl, 4 mM sodium acetate buffer, pH 5.3.

Notes préparatoires

Prepared from plasma that has been shown by certified tests to be negative for HBsAg and for antibodies to HIV and HCV.

Reconstitution

Following initial thaw, aliquot and freeze (-20°C).

Remarque sur l'analyse

homogeneous by SDS-PAGE

Informations légales

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

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Sandeep B Rajput et al.
Chinese medicine, 8(1), 18-18 (2013-09-10)
Asaronaldehyde (2, 4, 5-trimethoxybeznaldehyde) is an active component of Acorus gramineus rhizome. This study aims to evaluate the anti-Candida efficacy of asaronaldehyde and its three structural isomers, namely, 2, 3, 4-trimethoxybenzaldehyde, 3, 4, 5-trimethoxybenzaldehyde, and 2, 4, 6- trimethoxybenzaldehyde. Susceptibility
Asma Alshamari et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-24)
A series of derivatives of trans-3-(2,4,6-trimethoxyphenyl)4,5-dihydroisoxazolo-4,5-bis[carbonyl-(4'phenyl)thiosemicarbazide (9) and of trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro isoxazolo-4,5-bis(aroylcarbohydrazide) (10a-c) were synthesized from trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro-4,5-bis(hydrazenocarbonyl)isoxazole (8). The structures of the compounds were elucidated by both elemental and spectral (IR, NMR, and MS) analysis. Compound 9 shows activity against some
Lili Du et al.
Theranostics, 7(14), 3432-3445 (2017-09-16)
Small interfering RNA (siRNA) therapies have been hampered by lack of delivery systems in the past decades. Nowadays, a few promising vehicles for siRNA delivery have been developed and it is gradually revealed that enhancing siRNA release from endosomes into
Frederik Roelens et al.
European journal of medicinal chemistry, 40(10), 1042-1051 (2005-06-14)
Nine new (+/-)-8-alkyl-5,7-dihydroxy-4-(4-hydroxyphenyl)-3,4-dihydrocoumarins have been synthesized from 2,4,6-trimethoxybenzaldehyde via a short, efficient, and regioselective pathway, together with the unsubstituted analogue (+/-)-5,7-dihydroxy-4-(4-hydroxyphenyl)-3,4-dihydrocoumarin. The compounds were tested for estrogenic activity using a yeast-based estrogen screen. Weak estrogenicity was determined for seven members
Fatemeh Oroojalian et al.
Journal of controlled release : official journal of the Controlled Release Society, 288, 45-61 (2018-09-02)
In the current study, thermoresponsive poly(N-isopropylacrylamide)-doxorubicin (PNIPAM-DOX) hydrogel was synthesized and loaded into pH-responsive poly ethylene glycol)-2,4,6- trimethoxy benzylidene pentaerythritol carbonate (PEG-PTMBPEC) polymersomes in order to fabricate a smart thermo-pH stimuli responsive drug delivery system. Thermo-pH responsive polymersomal formulation of

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