Accéder au contenu
Merck
Toutes les photos(1)

Key Documents

SRP6516

Sigma-Aldrich

Albumin from human plasma

≥95% (SDS-PAGE)

Synonyme(s) :

Albumin protein, human Albumin, human Albumin protein, human plasma, human plasma Albumin proteinHSA, native Albumin, native Albumin protein

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(1)

About This Item

Numéro CE :
232-692-7
Code UNSPSC :
12352202
Nomenclature NACRES :
NA.32

Source biologique

human

Pureté

≥95% (SDS-PAGE)

Forme

lyophilized

Poids mol.

66 kDa

Conditionnement

pkg of 1G

Couleur

beige

Numéro d'accès UniProt

P02768 

Conditions d'expédition

wet ice

Température de stockage

−20°C

Informations sur le gène

human ... ALB(213)

Description générale

Human albumin is encoded by ALB gene that is mapped to human chromosome 4q. The gene is developmentally regulated and is synthesized by the liver. The encoded protein has a molar mass of 65,000 Da and consists of a single polypeptide chain of 585 amino acids.

Application

Albumin has been used in ion exchange chromatography to compare the albumin isolated from whole human plasma. It has been used to bind to phage clones in phage binding assay.

Actions biochimiques/physiologiques

Human albumin is a globular unglycosylated serum protein that makes up for more than half of the total plasma or serum proteins. It functions in the maintenance of COP (cellular oncotic pressure). It binds to hydrophobic organic anions such as, bilirubin, long-chain fatty acids and haematin and some cations such as magnesium and calcium. It also serves as a secondary or tertiary carrier for steroids, vitamin D and thyroxine. It is involved in the catabolism of prostaglandins and metabolism of certain endogenous substances, such as lipids, and eicosanoids. It acts as a plasma buffer and scavenges oxygen free radicals, thus reducing the pathological effects of certain inflammatory diseases. Mutation in the gene coding for albumin leads to familial dysalbuminaemic hyperthyroidism.

Forme physique

Lyophilized as a salt free solid.

Pictogrammes

Health hazard
GHS08

Mention d'avertissement

Danger

Mentions de danger

H334

Classification des risques

Resp. Sens. 1A

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Molecular structure of the human albumin gene is revealed by nucleotide sequence within q11-22 of chromosome 4.
Minghetti PP
The Journal of Biological Chemistry, 261, 6747-6757 (1986)
Isolation of albumin from whole human plasma and fractionation of albumin-depleted plasma.
Travis J
The Biochemical Journal, 157, 301-306 (1976)
Albumin binding as a general strategy for improving the pharmacokinetics of proteins.
Dennis MS
The Journal of Biological Chemistry, 277, 35035-35043 (2002)
Ziying Chen et al.
Cardiovascular research, 117(3), 820-835 (2020-04-08)
Calcific aortic valve disease (CAVD) is the most common heart valve disease in the Western world. It has been reported that zinc is accumulated in calcified human aortic valves. However, whether zinc directly regulates CAVD is yet to be elucidated.
The role of albumin in critical illness.
Nicholson JP
British Journal of Anaesthesia, 85, 599-610 (2000)
Afficher tous les articles scientifiques apparentés

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique