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Merck
CN

A8327

Bovine Serum Albumin solution

30%±2% in 0.85% sodium chloride, aseptically filled

Synonym(s):

Albumin solution from bovine serum, BSA solution

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About This Item

CAS Number:
9048-46-8
UNSPSC Code:
12352202
NACRES:
NA.27
MDL number:
MFCD00130384

Key Documents

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Product Name

Bovine Serum Albumin solution, 30%±2% in 0.85% sodium chloride, aseptically filled

biological source

bovine

sterility

aseptically filled

assay

28-32% protein basis (biuret)

form

solution

purified by

heat shock fractionation

does not contain

stabilizer or preservative

origin

USA origin

concentration

28-32% protein (biuret)
30%±2% in 0.85% sodium chloride

technique(s)

ELISA: suitable

UniProt accession no.

P02769

storage temp.

2-8°C

Quality Level

300

Gene Information

bovine ... ALB(280717)

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Application

Bovine Serum Albumin solution has been used:
  • as one of the experimental components to resemble the plasma-protein-rich acute respiratory distress syndrome (ARDS) edema liquid
  • to prepare embryos for fluorescent staining of the actin cytoskeleton
  • in tissue culture and neurite outgrowth assay

Biochem/physiol Actions

Serum Albumin regulates the osmotic pressure and pH of the blood. It transports various endogenous and exogenous compounds such as amino acids, drugs, steroids, and fatty acids. Bovine serum albumin (BSA) serves as a molecular weight standard, standard in vaccine preparation, and enzyme-linked immunosorbent assay (ELISA).

General description

Serum Albumin is a protein widely present in the circulating blood. Albumin has a helical structure with three domains that form a heart-like shape. It belongs to the four-member albumin superfamily.

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Regulatory Information

含少量动物源组分生物产品
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Certificates of Analysis (COA)

Lot/Batch Number
0000513494
0000513494
0000456795
0000456795
0000455876

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Coronaviruses make use of a large envelope protein called spike (S) to engage host cell receptors and catalyze membrane fusion. Because of the vital role that these S proteins play, they represent a vulnerable target for the development of therapeutics.
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Current coronavirus (CoV) vaccines primarily target immunodominant epitopes in the S1 subunit, which are poorly conserved and susceptible to escape mutations, thus threatening vaccine efficacy. Here, we use structure-guided protein engineering to remove the S1 subunit from the Middle East
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