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BSAV-RO

Roche

Bovine Serum Albumin

≥98.5%, New Zealand origin

Synonym(s):

Bovine Serum Albumin Fraction V

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About This Item

UNSPSC Code:
12352202
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biological source

bovine

Quality Level

100

Assay

≥98.5%

form

lyophilized

mol wt

Mr =68 kDa

packaging

pkg of 1 kg (10735108001)
pkg of 100 g (10735086001)
pkg of 50 g (10735078001)
pkg of 500 g (10735094001)

manufacturer/tradename

Roche

origin

New Zealand origin

technique(s)

ELISA: suitable
Southern blotting: suitable
western blot: suitable

impurities

<0.0003 Lithium (Flame photometry)
<0.001 Iron (bathophenanthraline)
<0.002 P (inorganic)
<0.003 Heavy metals (as Pb)
<0.003 Magnesium (xylidyl blue)
<0.005 Glycerol (enzyme)
<0.006 potassium (Flame photometry)
<0.02 Calcium ( o-cresolphthalein)
<0.05 glucose (enzyme)
<0.1 L-lactate
<0.15 chloride (mercurom)
<0.5 Sodium (flame photometry)
<100 microorganisms (organism/g)
<5 water

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1 of 4

This Item
81053381053N810535
Bovine Serum Albumin &#8805;98.5%, New Zealand origin

BSAVRO

Bovine Serum Albumin

Bovine Serum Albumin Fraction V pack of 100&#160;g

810533

Bovine Serum Albumin Fraction V

Bovine Serum Albumin Fraction V pack of 10&#160;g

81053N

Bovine Serum Albumin Fraction V

Bovine Serum Albumin Fraction V pack of 5&#160;kg

810535

Bovine Serum Albumin Fraction V

assay

≥98.5%

assay

≥98% (purity)

assay

≥98% (purity)

assay

≥98% (purity)

technique(s)

ELISA: suitable, western blot: suitable, Southern blotting: suitable

technique(s)

blood typing: suitable ( )

technique(s)

blood typing: suitable ( )

technique(s)

blood typing: suitable ( )

origin

New Zealand origin

origin

USA origin

origin

USA origin

origin

USA origin

biological source

bovine

biological source

bovine serum

biological source

bovine serum

biological source

bovine serum

Quality Level

100

Quality Level

300

Quality Level

300

Quality Level

300

form

lyophilized

form

lyophilized powder

form

lyophilized powder

form

lyophilized powder

General description

For standard applications.

Application

Bovine Serum Albumin Fraction V is suitable for standard applications such as:
  • Stabilizer to prevent proteolysis and denaturation of enzymes and other proteins, especially when the proteins are present in low concentrations.[1]
  • Buffer component in immunochemistry, biochemistry, cell biology, or molecular biology
  • Reducing agent
  • Protein blocker for saturation of protein binding sites in ELISAs, Southern blots, and western blots[2]
  • Media supplement for media that require addition of protein
  • Carrier protein
  • Standard protein in gel electrophoresis and protein determination[3]

Quality

Purity: ≤95% protein, ≤5% H2O; electrophoretically homogeneous
Contaminants: <0.5% Na (flame photometric), <0.006% K (flame photometric), <0.0003% Li (flame photometric), <0.02% Ca (o-cresolphthalein), <0.003% Mg (xylidyl blue), <0.003% heavy metals (as Pb), <0.001% Fe (bathophenanthroline), <0.002% Pi, <0.05% glucose (enzymatic), <0.005% glycerol (enzymatic), <0.025% L-lactate (enzymatic)

Preparation Note

Storage conditions (working solution): In solution, albumin is stable for about three months at -15 to -25 °C.

Other Notes

For life science research only. Not for use in diagnostic procedures.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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    Certificates of Analysis (COA)

    Lot/Batch Number
    69453727
    64758436
    64758430
    64758425
    64758421

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    Laurent Berchebru et al.
    Journal of microbiological methods, 105, 141-145 (2014-07-20)
    Test and evaluation of engineered biothreat agent detection systems ("biodetectors") are a challenging task for government agencies and industries involved in biosecurity and biodefense programs. In addition to user friendly features, biodetectors need to perform both highly sensitive and specific
    Paulina Krzysica et al.
    Animals : an open access journal from MDPI, 12(21) (2022-11-12)
    Cytokines like interferon (IFN)-γ, interleukin (IL)-2, IL-6, IL-10, and IL-12p40 are important biomarkers for characterizing the nature and strength of immune responses. It is important to be able to quantify the cytokines at the protein level in biological samples. Quantification
    Leonie Kollenstart et al.
    Scientific reports, 11(1), 12795-12795 (2021-06-19)
    The collection of known posttranslational modifications (PTMs) has expanded rapidly with the identification of various non-acetyl histone lysine acylations, such as crotonylation, succinylation and butyrylation, yet their regulation is still not fully understood. Through an unbiased chromatin immunoprecipitation (ChIP)-based approach
    Francis K Y Siu et al.
    Nature protocols, 3(1), 51-58 (2008-01-15)
    Southwestern blotting is used to investigate DNA-protein interactions. The advantage of this technique over other related methods such as electrophoretic mobility shift assay (EMSA) and DNA footprinting is that it provides information regarding the molecular weight of unknown protein factor.
    Mariko Kuse et al.
    The Journal of reproduction and development, 59(4), 346-352 (2013-04-09)
    Cortisol (Cr), the most important glucocorticoid (GC), is well known to suppress uterine prostaglandin F2α (PGF) production. However, the details of the regulatory mechanisms controlling the cyclic changes in endometrial PGF production remain unclear. Here we investigated the expression of
    View All Related Papers

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