Monoclonal Antibodies
All antibodies are purified on a Protein A column (Ey et al., 1978)1 using the low-salt method.
The antibodies are supplied at a concentration requiring ~1:1000 dilution for Western blotting. All antibodies are stored in Phosphate Buffered Saline (PBS) pH 7.2. Store at -20°C. (stable for at least 12 months undiluted).
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7F11 Gyr A
This is an IgG2b monoclonal antibody raised against the N-terminal domain of E. coli Gyr A produced from tissue culture supernatant derived from mouse hybridoma cells.
Technical Documents
4D3 Gyr A
This is an IgG2b monoclonal antibody raised against the C-terminal domain of E. coli Gyr A produced from tissue culture supernatant derived from mouse hybridoma cells.
Technical Documents
9G8 Gyr B
This is an IgG2a monoclonal antibody raised against the C-terminal domain of E. coli Gyr B produced from tissue culture supernatant derived from mouse hybridoma cells.
Technical Documents
7D3 Gyr B
This is an IgG2a monoclonal antibody raised against the N-terminal domain of E. coli Gyr B produced from tissue culture supernatant derived from mouse hybridoma cells.
Technical Documents
References
- Ey, P.L., S.J., & Jenkin, C.R. (1978). Isolation of pure IgG1, IgG2a, and IgG2b immunoglobulins from mouse serum using Protein A sepharose. Immunochemistry. 15: 429-436
- Harlow, E. & Lane, D (1988). Antibodies: a laboratory manual. Cold Spring Harbor Laboratory press. Cold Spring Harbor
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我最近用乳化交联法制备壳聚糖盐酸盐微球，药物是水不溶性(醋酸共晶体)，将药物乙醇溶液加入到3%壳聚糖盐酸盐溶液中，混合均匀，加入到含2%span80的液体石蜡，油水比6:1，乳化半小时，加入1.5ml戊二醛，交联30min，离心，用石油醚，丙酮各洗两次，干燥，得微球。
但是我研磨微球，用乙醇溶解药物，超声3h，在紫外下根本检测不到药物，包封率就没法算，我测了药物在石油醚和丙酮中都有一定的溶解度，洗的时候溶剂层也有药物的颜色，是不是微球中的药物都被洗了出来？还是只是把游离的药物洗了出来？药物根本就没被包进去？但是药物在有机溶剂中都有一定的溶解度，我该怎么做？有大神愿意告知一二吗？？？？
版主shitou0307留言:
因为你还没学会怎么提问
Rainbow Calibration ParticlesSPHEROBD，但惊奇地发现BD这个目录里面居然也家sphero的rainbow微球，两者啥关系？Life Flow Cytometer Alignment & Linearity BeadsBangs LabThermo ScientificPolysicence Flow Check® Calibration Particles & Kits
1、该制剂为肌肉注射；
2、制备该微球过程中用到了二氯甲烷、乙醇、正庚烷、二甲基硅油。国家药典有机溶剂残留规定：二氯甲烷残留限度为0.06%；乙醇残留限度为0.5%；正庚烷残留限度0.5%；二甲基硅油药典中还为収载。目前自制微球的二氯甲烷残留约0.2%左右，正庚烷残留1.0%左右，乙醇残留0.3%左右，二甲基硅油暂未检测。很明显：二氯甲烷和正庚烷超标。后来测了一下原研制剂的有机溶剂残留：二氯甲烷残留约0.1%左右，正庚烷残留1.5%左右，乙醇残留0.2%左右。本人也制剂新手，请各位大神帮帮忙，积极发言。我这个长效缓释PLGA微球制剂中有机溶剂残留限应该定多少合适，我后期优化工艺时对上述有机残留应该控制到多少一下合适。
最近想做小鼠微循环的检测，参照了DissectingtheEffectsofIschemiaandReperfusionontheCoronaryMicrocirculationinaRatModelofAcuteMyocardialInfarction这篇文献，想做荧光微球。但是不知道这个荧光微球具体该怎么用，要怎么处理，文献写的不详细，问了厂家也是不太清楚，希望有大神可以指点，提供详细些的实验步骤。多谢。
各位大侠，微球作为局部缓释药物，怎么储藏呢，微球不是散开的吗，怎么形成像凝胶状的呢
