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CATALOG<br />

NUMBER<br />

BASIC YELLOW 11<br />

C.I. 48055<br />

C21H25ClN2O2<br />

RT MW 372.9 4208-80-4<br />

152632 50 g<br />

100 g<br />

BATHOCUPROINE<br />

(2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline)<br />

Crystalline<br />

C26H20N2 MW 360.5<br />

RT 4733-39-5<br />

150424 100 mg<br />

500 mg<br />

1 g<br />

BATHOCUPROINE DISULFONIC ACID<br />

(2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline disulfonate)<br />

Disodium Salt<br />

Crystalline<br />

Pale yellow crystals. Used as a stain for proteins in polyacrylamide<br />

gels 1 ; for determination of iron 2 and copper 3 ; and uric acid <strong>by</strong> automated<br />

procedures.<br />

Ref.: 1. Graham, G., et al., Anal. Biochem., 11: 88, 434, (1978); 2.<br />

Landers, J.U. and Zak, B., Am. J. Clin. Pathol., 29: 590, (1958); 3. Clin.<br />

Chim. Acta, 3: 328, (1958).<br />

C26H18N2O6S2Na2<br />

RT MW 564.6 52698-84-7<br />

100868 100 mg<br />

1 g<br />

5 g<br />

BATHOPHENANTHROLINE<br />

(4,7-Diphenyl-1,10-phenanthroline)<br />

Crystalline<br />

Used for colorimetric iron determinations.<br />

C24H16N2<br />

RT MW 332.41 1662-01-7<br />

190157 100 mg<br />

500 mg<br />

1 g<br />

BATHOPHENANTHROLINE DISULFONIC ACID<br />

Disodium salt<br />

Crystalline<br />

Water soluble.<br />

Useful for aqueous iron determination without need for solvent<br />

extraction.<br />

C24H14N2S2O6Na2<br />

RT MW 554.6 52746-49-3<br />

150112 100 mg<br />

1 g<br />

5 g<br />

Biochemicals<br />

Alphabetical List<br />

CATALOG<br />

NUMBER<br />

BATROXOBIN<br />

(EC 3.4.21.29)<br />

From: Bothrops atrox<br />

Activity: 120 BU/mg<br />

Unit Definition: the clotting time of bovine fibrinogen following the<br />

addition of ~0.2 ml batroxobin is recorded and converted into batroxobin<br />

units (BU) using the standard curve developed with the first British<br />

Standard, lot 75/527.<br />

Batroxobin coverts fibrinogen to fibrin through the cleavage of the Arg-<br />

Gly bonds of the-chain, resulting with fibrinopeptide A release. It<br />

will<br />

not be inactivated <strong>by</strong> thrombin inhibitors.<br />

194102 300 µg<br />

821821<br />

www.mpbio.com<br />

()-BAY K 8644<br />

(1,4-Dihydro-2,6-dimethyl-5-nitro-4-[2-(trifluoromethyl)-phenyl]-3-<br />

pyridine-carboxylic acid methyl ester)<br />

C16H15F3N2O4<br />

0 TO 5°C MW 356.3 98791-67-4<br />

153628 1 mg<br />

5 mg<br />

Bbs I 5’...GAAGAC(N)2/...3’<br />

From: Bacillus laterosporus<br />

Activity: 1,000 to 10,000 units/ml.<br />

Supplied in 150 mM KCl, 10 mM Tris-HCl pH 7.5, 0.1 mM EDTA, 1 mM<br />

dithiothreitol, 200 g/ml acetylated BSA, and 50% glycerol.<br />

-20°C<br />

159399 200 U<br />

Bbv I 5’...GCAGC(N)8/12/...3’<br />

Isolated from Bacillus brevis<br />

(ATCC 9999)<br />

Activity: 200 to 2,000 units/ml.<br />

Supplied in 50 mM KCl, 10 mM Tris-HCl pH 7.4, 0.1 mM EDTA, 1 mM<br />

dithiothreitol, 200 g/ml BSA and 50% glycerol.<br />

Ref.: Gingeras, T.R., Milazzo, J.P. and Roberts, R.J., Nucleic Acids<br />

Res., 5: 4105-4127, (1978). Schildkraut,I., unpublished observations.<br />

-20°C<br />

153804 150 U<br />

BCIP/INT LIQUID SUBSTRATE<br />

(5-Bromo-4-chloro-3-indolyl Phosphate/p-Iodonitrotetrazolium)<br />

Stabilized Chromogen Solution<br />

Similar to BCIP/NBT but results in an intense orange color. Concentration:<br />

0.46 mmol/liter BCIP; 0.79 mmol/liter INT.<br />

RT<br />

821819 100 ml<br />

BCIP/TNBT LIQUID SUBSTRATE<br />

(5-Bromo-4-chloro-3-indolyl Phosphate/Tetranitroblue Tetrazolium)<br />

Stabilized Chromogen Solution<br />

Similar to BCIP/NBT Plus but is more sensitive and produces an intense<br />

purple color. It is highly useful in double antibody staining procedures<br />

when used with BCIP/INT where phosphatase labeled antibodies are<br />

preferred. Concentration: 0.452 mmol/liter BCIP; 0.432 mmol/liter TNBT.<br />

RT<br />

100 ml<br />

90<br />

One Call. One Source. A World of Biotechnology Reagents. www.mpbio.com

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