What's the difference between cacodyl and tetramethyldiarsine?
Cacodyl
Definition:
(n.) Alkarsin; a colorless, poisonous, arsenical liquid, As2(CH3)4, spontaneously inflammable and possessing an intensely disagreeable odor. It is the type of a series of compounds analogous to the nitrogen compounds called hydrazines.
Example Sentences:
(1) The results indicate that in 10(-3) M sodium cacodylate the binding constant of BAD is 1.8 x 10(3) M-1.
(2) Protein aggregation is dependent on the concentration of background electrolyte since in the range 10-150 mM sodium cacodylate alternative stabilisation of dimeric and trimeric complexes was observed by both NMR and analytical ultracentrifugation.
(3) Yeast cells were fixed for 20 min in cold 1% glutaraldehyde buffered with 50 mM TES buffer to pH 7.0 and then incubated for 80 min with 1.2 mM L-alanyl-L-proline-4-methoxy-2-naphthylamide (Ala-Pro-MNA) or Lys-Pro-MNA as cytochemical substrates plus 0.06% hexazonium p-rosaniline (HPR) buffered with 160 mM cacodylate to pH 7.0.
(4) The two-step method uses cationic cacodylate iron colloid which is substituted with Tween 20 at an OD460 nm = 0.5, followed by Perls' reaction with acid potassium ferrocyanide.
(5) It was noted that the microtubular structure, which could not be demonstrated even by alcian blue or cationic ferric hydroxide colloid stabilized with cacodylate (Fe-CaC), was clearly detected with anti-EMA.
(6) The melting of chromatin was followed in 5 mM sodium-cacodylate buffer (pH 7.0)+1.5-10(-4) M EDTA containing increasing concentrations of urea.
(7) 260, 7619-7627); and (ii) an alpha 2----3 sialyltransferase that was efficiently solubilized by 0.2% Triton X-100 and required divalent metal ions and 0.3% Triton CF-54 for optimal activity at pH 5.9 in cacodylate buffer.
(8) Utilizing morphometry of electron micrographs of nerves of rat fixed with different schedules of fixation it was concluded that: irrespective of the fixative, fixation at low temperature is associated with markedly low densities of microtubules (MT) of myelinated and of unmyelinated fibers; of the various fixatives tested 2% glutaraldehyde in 0.1 M cacodylate buffer without 0.025 M CaCl2 was associated with the highest density of MT of myelinated fibers and the addition of 0.025 M CaCl2 to a 2% glutaraldehyde fixative solution is associated with abnormally low densities of MT in myelinated and unmyelinated fibers.
(9) Tissues were washed in buffer, then stained in medium containing glucose, diaminobenzidine HCl, and dimethylsulfoxide in 0.1 M cacodylate buffer.
(10) The cacodylate molecule is decomposed to As(V) by heating with Mg(NO3)2.6H20; As(V) is then chemically reduced to As(III) and polarographed in 1M HCl supporting electrolyte.
(11) The midpoint was pCa 8.25 for the former protein and 6.80 for the latter protein in 0.1 M KCl, 50 mM Na-cacodylate-HCl (pH 7.0); and pCa 7.90 for the former protein and 6.70 for the latter protein in the presence of 3 mM MgCl2 in the same solvent system.
(12) In each transport mode, the intercellular spaces were measured after immersion in a series of fixatives in which the concentration of buffer (sodium cacodylate) was increased.
(13) We have found that when a buffer utilized for in vitro polymerization of microtubules, i.e., 1 mM guanosine triphosphate, 1 mM MgSO4, 2 mM ethylene glycol bis(beta-aminoethyl ether)-N, N'-tetraacetic acid 100 mM piperazine-N,N'-bis(2-ethanesulfonic acid), pH 6.9 polymerization mix, was used in the glutaraldehyde prefixation regimen instead of classical fixative buffers, i.e., isotonic cacodylate or phosphate buffer, the following features were observed in thin-sections of the cytoplasm of interphase HeLa cells: (a) a greater than 2-fold increase in total microtubule contour length, (b) a 2-fold increase in a number of microtubules greater than or equal to 1 mu long, (c) an enhanced association of microtubules with cytoplasmic organelles, and (d) an increased clustering of 100 A filaments located in a perinuclear region of the cell.
(14) The isolated, maximally vasodilated rat hindquarter preparation was used to determine how fixation of the vascular bed (glutaraldehyde, 2.5% in 0.05 M Na-cacodylate with dextran 40 g X 1-I) affected transcapillary filtration and diffusion events, as well as macromolecular transfer, measured as transport of water (CFC), of small solutes (PS) and of 125I-albumin.
(15) Tissue samples taken from the left auricular myocardium of four pig hearts at 0, 0.5, 1.5, 3.5, 6, 12 and 24 hours post mortem were fixed for 24 hours by immersion in 2.5 per cent cacodylate buffered glutaraldehyde (pH 7.4).
(16) At pH 7.2, 24 degrees C and in 5mM sodium cacodylate buffer solution, this binding increases the lifetime of the diol epoxide by a factor of nearly 3.
(17) While in pure water (cacodylate buffer pH 7.0, NaCl 0.1 M) they are respectively +388 and +265 mV, in 50% dimethylsulfoxide at 25 degrees C they decrease to +112 and +208 mV.
(18) Optimum pH was 6.8 in cacodylate buffer, and Km values were 2 microM for lactotriaosylceramide and 29 microM for UDP-galactose.
(19) Nine pesticides tested by the oral route (bufencarb, cacodylic acid, dialifor, deltamethrin, dicamba, diquat, quintozene, phoxim, pyrazon) and four tested by the dermal route (bufencarb, chlordimeform, dichlofenthion, leptophos) were more toxic to females than to males whereas famphur and 2,4,5-T (oral route) were less toxic to females.
(20) At the end of the time period, the cornea was flooded with 4% glutaraldehyde, buffered with cacodylate, pH 7.4, and kept moist until removed.