WJ101由15kDa~150kDa范围的9个蛋白条带组成(15kDa、20kDa、25kDa、35kDa、40kDa、50kDa、70kDa、100kDa、150kDa)。WJ102、WJ103和WJ106由10kDa~250kDa范围的11个蛋白条带组成(10kDa、15kDa、20kDa、25kDa、35kDa、40kDa、50kDa、70kDa、100kDa、150kDa、250kDa)。由低到高的分子量范围可监测电泳过程中的蛋白分离情况、判断目标蛋白的分子量，并且可以监测Western Blot实验中的转膜效率。25kDa、70kDa两条带结合有红色或绿色染料，更便于实时观察电泳进程、判断蛋白分子量，其中WJ106特别适用于近红外荧光成像系统。
缓冲液成分：62.5mM Tris-HCl(pH7.5/25℃)，1mM EDTA，2%(W/V)SDS，10mM DTT，33%(W/V)glycerol。
| WJ101(15 kDa~150 kDa)250 μL×2 | WJ101L(15 kDa~150 kDa)250 μL×10 |
| WJ102(10 kDa~250 kDa)250 μL×2 | WJ102L(10 kDa~250 kDa)250 μL×10 |
| WJ103(10 kDa~250 kDa)250 μL×2 | WJ103L(10 kDa~250 kDa)250 μL×10 |
| WJ106(10 kDa~250 kDa)250 μL×2 | WJ106L(10 kDa~250 kDa)250 μL×10 |
| 注：WJ106 系列适用于近红外荧光成像系统。 | |
高准确性
蛋白条带分子量准确性与知名进口品牌相当，甚至略有优势方便使用
蛋白条带分布合理，便于参照低杂交反应
条带蛋白去除蛋白质标签，最大程度降低抗体与其非特异性结合高性价比
与其它品牌同款产品相比，性价比非常高
加样前在室温放置数分钟，解冻后，轻轻摇匀，以确保溶液混合均匀；
取用适量体积加样于凝胶孔，推荐用量为2~5μL/孔，可根据具体情况适当增减。
取用结束，盖上管盖，放回4℃或-20℃。
注：以上样5μL为例，WJ101、WJ102、WJ103及WJ106每个条带蛋白含量约为1μg~3μg。
不同电泳缓冲条件下，WJ101、WJ102、WJ103 及 WJ106 各条带指示分子量(kDa)
1. 本品已包含上样缓冲液，直接使用，不可加热煮沸；
2. 为避免反复冻融及污染，可将本产品分装后，-20℃保存；
3. 预染蛋白质分子量标准仅用于分子量的近似参考，批次间差异约为5%；
4. 若使用近红外荧光成像系统，请选用WJ106；
5. 在低浓度凝胶中，低分子量条带将会与前沿共迁移而无法分出；
6. 在不同凝胶和缓冲液系统中，预染蛋白质的迁移率会有所差别，可用非预染蛋白质分子量标准进行校正，并按校正后的结果正常使用；
7. 蛋白Marker可能会与抗体发生非特异性结合，可以降低抗体浓度、减少孵育时长，以及减小蛋白Marker上样量来进行优化；
8. 为了您的安全和健康，请穿实验服并戴一次性手套操作；
9. 本产品仅限科研使用。
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