化工社化工社 化学情報印刷レポート · 研究参考用
4-((4-Isothiocyanatophenyl)azo)-N,N-dimethylaniline → Erythrosine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-((4-Isothiocyanatophenyl)azo)-N,N-dimethylaniline | HCID 82084 | — |
| 反応物 | Erythrosine isothiocyanate | HCID 188262 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Sodium Bicarbonate | HCID 516892 | — |
| 生成物 | Erythrosine | HCID 3259 | — |
反応手順
Antibody (2 mg) was dissolved in 2 ml of 1% NaHCO3 pH 8.6, and a 20-ul aliquot of a solution of 1 mg/ml 4-dimethylaminoazobenzene-4'-isothiocyanate in dimethylformamide (DMF) added. The mixture was stirred overnight, then desalted on a Sephadex G-25 (coarse) column (1×30 cm). The ultraviolet-and visible spectrum of the conjugate was compared to that of DAB and antibody alone, to determine the degree of substitution. An erythrosin-antibody conjugate was prepared the same way, except the concentration of the erythrosin-isothiocyanate in DMF was 2.5 mg/ml.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05376556 |
| 出典データセット | uspto-grants-1994_12 |
| ORD ID | ord-4d2f18fb3a154ed6a0857b5a9e723a44 |
| 出典メモ | uspto-grants-1994_12 |