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B2064

Sigma-Aldrich

Bovine Serum Albumin

heat shock fraction, Australia origin, protease free, low fatty acid, low IgG, pH 7, ≥98%

Synonym(s):

Bovine Serum Albumin, Albumin bovine serum, BSA, Bovine albumin

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About This Item

CAS Number:
EC Number:
MDL number:
UNSPSC Code:
12352202
NACRES:
NA.27
Pricing and availability is not currently available.
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biological source

bovine

assay

≥98%

form

powder

mol wt

~66 kDa

purified by

heat shock fractionation

origin

Australia origin

fatty acid content

<0.05%

technique(s)

immunofluorescence: suitable

impurities

≤0.05% IgG

pH

7

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1 of 4

This Item
GF88927543GF86135160GF47768596
Iron rod, 1000mm, diameter 2.0mm, as drawn, 99.95%

GF90625181

Iron

Iron rod, 1000mm, diameter 2.0mm, as drawn, 99.99+%

GF88927543

Iron

Iron rod, 500mm, diameter 2.0mm, as drawn, 99.95%

GF86135160

Iron

Iron rod, 500mm, diameter 2.0mm, as drawn, 99.99+%

GF47768596

Iron

form

rod

form

rod

form

rod

form

rod

manufacturer/tradename

Goodfellow 906-251-81

manufacturer/tradename

Goodfellow 889-275-43

manufacturer/tradename

Goodfellow 861-351-60

manufacturer/tradename

Goodfellow 477-685-96

assay

≥99.95%

assay

≥99.99%

assay

≥99.95%

assay

99.99%

density

7.86 g/mL at 25 °C (lit.)

density

7.86 g/mL at 25 °C (lit.)

density

7.86 g/mL at 25 °C (lit.)

density

7.86 g/mL at 25 °C (lit.)

bp

2750 °C (lit.)

bp

2750 °C (lit.)

bp

2750 °C (lit.)

bp

2750 °C (lit.)

resistivity

9.71 μΩ-cm

resistivity

9.71 μΩ-cm

resistivity

9.71 μΩ-cm

resistivity

9.71 μΩ-cm

General description

Bovine serum albumin (BSA) is made up of 583 amino acids, with no carbohydrates.[1][2] It is a water-soluble protein with a molecular weight of 66.4kDa. Six α-helices form three homologous domains of BSA. Depending on pH, it undergoes reversible conformational isomerization. The native structure of BSA becomes reactive and flexible on heating.[3] BSA acts as a model protein in various studies, such as immunodiagnostic procedures, cell culture media and clinical chemistry. It is also relevant in foods containing bovine milk or meat.[2]
Appl- Bovine serum albumin has been used as a supplement of phosphate buffered saline (PBS) to store brain tissue sections.[4] It has also been used as a blocking agent for cells for immunofluorescence analysis.[5][6]

Biochem/physiol Actions

Certain conformational and primary-sequence epitopes of BSA are suspected allergens in human beef and milk allergies.

Features and Benefits

  • Australia origin
  • Fatty acid free / ultra-low fatty acid content (≤ 0.05%)
  • Protease-free
  • Low IgG content (≤ 0.05% IgG by Ouchterlony Titer)

Preparation Note

Serum albumin may be referred to as Fraction V. This naming convention is taken from the original Cohn method of fractionating serum proteins using cold ethanol precipitation. Serum albumin was found in the fifth ethanol fraction using Cohn′s method. Since then, the term "Fraction V" has been used by some to describe serum albumin regardless of the method of preparation. Others have used this term to describe serum albumin purified by ethanol fractionation methods that have been highly modified since the original Cohn method was described. Sigma-Aldrich manufactures and distributes serum albumins purified from a variety of primary methods including the true Cohn fractionation method, modified ethanol fractionation methods, heat shock and chromatography. Additional purification steps may include crystallization or charcoal filtration.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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    Mathilde Dusséaux et al.
    Gastroenterology, 153(6), 1647-1661 (2017-08-31)
    Hepatitis B virus (HBV) infects hepatocytes, but the mechanisms of the immune response against the virus and how it affects disease progression are unclear. We performed studies with BALB/c Rag2-/-Il2rg-/-SirpaNODAlb-uPAtg/tg mice, stably engrafted with human hepatocytes (HUHEP) with or without
    Farhad Khosravi et al.
    Nanotechnology, 27(13), 13LT02-13LT02 (2016-02-24)
    We demonstrate the rapid and label-free capture of breast cancer cells spiked in buffy coats using nanotube-antibody micro-arrays. Single wall carbon nanotube arrays were manufactured using photo-lithography, metal deposition, and etching techniques. Anti-epithelial cell adhesion molecule (EpCAM) antibodies were functionalized

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