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Recombinant Human Apolipoprotein A-I/ApoAI Protein (His Tag, E. coli)– MSE Supplies LLC

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Recombinant Human Apolipoprotein A-I/ApoAI Protein (His Tag, E. coli)

SKU: PKSH032081-50

  • £9500
  • Save £1000



Recombinant Human Apolipoprotein A-I/ApoAI Protein (His Tag, E. coli)

 

SKU # PKSH032081
Expression Host E.coli

 

 

Description

Synonyms APOA1, Apo-AI, ApoA-I, Apolipoprotein A-I, Apolipoprotein A1
Species Human
Expression Host E.coli
Sequence Arg19-Gln267
Accession P02647
Calculated Molecular Weight 30.2 kDa
Observed Molecular Weight 28 kDa
Tag C-His
Bio-activity Not validated for activity
  

 

Properties

Purity > 95 % as determined by reducing SDS-PAGE.
Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from a 0.2 μm filtered solution of 20mM PB, 6% Sucrose, 4% Mannitol, 50mM Nacl, 0.05% Tween 80, pH7.4.
Normally 5% - 8% trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.



Background

Apolipoprotein A1 (APOA1) is a secreted protein which belongs to the Apolipoprotein A1/A4/E family. APOA1 is the major protein component of high density lipoprotein (HDL) in plasma. APOA1 plays a critical role in various biological processes; such as Cholesterol metabolism; Lipid metabolism and transport; Steroid metabolism. APOA1 promotes cholesterol efflux from tissues to the liver and thus helps to clear cholesterol from arteries. Defects in this gene resulted in HDL deficiencies; including Tangier disease (TGD); systemic non-neuropathic amyloidosis; premature coronary artery disease; hepatosplenomegaly and progressive muscle wasting and weakness. In addition; ApoA-I is implicated in the anti-endotoxin function of HDL via interaction with lipopolysaccharide or endotoxin.