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B0508

Sigma-Aldrich

Brain acetone powder bovine

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biological source

bovine

form

powder

technique(s)

tissue culture: suitable

storage temp.

−20°C

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L0756M6890L8376
Brain acetone powder bovine

Sigma-Aldrich

B0508

Brain acetone powder bovine

Lung acetone powder from rabbit

Sigma-Aldrich

L0756

Lung acetone powder from rabbit

Muscle acetone powder from rabbit

Sigma-Aldrich

M6890

Muscle acetone powder from rabbit

Liver acetone powder from pigeon

Sigma-Aldrich

L8376

Liver acetone powder from pigeon

form

powder

form

powder

form

solid

form

powder

technique(s)

tissue culture: suitable

technique(s)

-

technique(s)

-

technique(s)

-

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

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

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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)
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).
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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