Document Finishing by Wordzworth
Document Finishing by Wordzworth
Document Finishing by Wordzworth
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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