カタログ製品コード : C-E14966h
ELISA kit for B-cell lymphoma/leukemia 11B
24T | ¥89,900 | (¥3,746/T) (税別) |
48T | ¥103,100 | (¥2,148/T) (税別) |
96T | ¥122,800 | (¥1,279/T) (税別) |
標準納期 : 2週間 |
カタログ製品コード : C-E14966h
ELISA kit for B-cell lymphoma/leukemia 11B
24T | ¥89,900 | (¥3,746/T) (税別) |
48T | ¥103,100 | (¥2,148/T) (税別) |
96T | ¥122,800 | (¥1,279/T) (税別) |
標準納期 : 2週間 |
メーカー名 | 遺伝子名 | 種交差性 | 測定範囲 | サンプル量 | 適用サンプル | ドキュメント |
---|---|---|---|---|---|---|
EIAab | BCL11B | Human | 78-5000 pg/mL | 100 μl | 血清、血漿、尿、組織ホモジネート、細胞培養上清等 |
■保存方法 :
一時保存の場合
TMB:4℃
試薬類:バイアルに記載の温度
長期保存の場合
-20℃
■測定原理 :
The microtiter plate provided in this kit has been pre-coated with an antibody specific to BCL-11B. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for BCL-11B and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain BCL-11B, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of BCL-11B in the samples is then determined by comparing the O.D. of the samples to the standard curve.
■構成内容 :
Reagent | Quantity |
Assay plate | 1 |
Standard | 2 |
Sample Diluent | 1 × 20ml |
Assay Diluent A | 1 × 10ml |
Assay Diluent B | 1 × 10ml |
Detection Reagent A | 1 × 120μl |
Detection Reagent B | 1 × 120μl |
Wash Buffer(25 x concentrate) | 1 × 30ml |
Substrate | 1 × 10ml |
Stop Solution | 1 × 10ml |
Plate sealer for 96 wells | 5 |
Instruction | 1 |
■キーワード :
Homo sapiens,Human,B-cell lymphoma/leukemia 11B,BCL-11B,B-cell CLL/lymphoma 11B,COUP-TF-interacting protein 2,Radiation-induced tumor suppressor gene 1 protein,hRit1,BCL11B,CTIP2,RIT1
■ターゲット情報 :
Tumor-suppressor protein involved in T-cell lymphomas. May function on the P53-signaling pathway. May be a key regulator of both differentiation and survival during thymocyte development. Repress transcription through direct, TFCOUP2-independent binding to a GC-rich response element.