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Key Documents

B0508

Sigma-Aldrich

Brain acetone powder bovine

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About This Item

UNSPSC Code:
12352202
NACRES:
NA.25

biological source

bovine

Quality Level

form

powder

technique(s)

tissue culture: suitable

storage temp.

−20°C

Application

Brain acetone powder bovine may be used in studies tissue-specific genes leading to the expression of proteins important for the analysis of immunoreactivity, disease pathogenesis and drug targeting.
Has been used as a crude source of calmodulin.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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T B Ng
The International journal of biochemistry, 24(4), 653-656 (1992-04-01)
1. Bovine cerebral hemispheres were extracted with an acidic medium (acetone-water-hydrochloric acid mixture, 40:5:1 by volume, pH 1.8). The precipitate which formed upon addition of a copious volume of cold acetone to the extract was designated acid acetone powder (AAP).
W M Pardridge et al.
Molecular and cellular neurosciences, 1(1), 20-28 (1990-08-01)
Tissue-specific gene expression within the brain capillary endothelium, which makes up the blood-brain barrier (BBB) in vivo, may lead to the production of brain capillary-specific proteins (BSPs). BSPs were defined in the present study by immunocytochemistry and Western blotting using
Affinity chromatographic isolation of calmodulin from bovine-brain acetone powder.
C R Caldwell et al.
Analytical biochemistry, 116(2), 325-330 (1981-09-15)
Eric V Shusta et al.
Molecular & cellular proteomics : MCP, 1(1), 75-82 (2002-07-04)
The cloning of genes expressing proteins that are differentially expressed in the organ microvasculature has the potential to address a variety of problems ranging from the analysis of disease pathogenesis to drug targeting for particular tissues. This study describes a

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