WesternBreeze™ 化学发光试剂盒,抗山羊
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Invitrogen™

WesternBreeze™ 化学发光试剂盒,抗山羊

WesternBreeze® Chemiluminescent Kits detect proteins that have been immobilized on membranes (nitrocellulose or PVDF) following western transfer or bound directly了解更多信息
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货号数量
WB71081 kit
货号 WB7108
价格(CNY)
8,366.00
1 kit
添加至购物车
数量:
1 kit
价格(CNY)
8,366.00
1 kit
添加至购物车
WesternBreeze® Chemiluminescent Kits detect proteins that have been immobilized on membranes (nitrocellulose or PVDF) following western transfer or bound directly from solution (dot blots). Detection is accomplished with a ready-to-use CDP-Star® chemiluminescent substrate for alkaline phosphatase. Protein bands can be captured either by X-ray film or CDP-Star® compatible imaging system. WesternBreeze® Chemiluminescent Kit offers:

• High specificity, clean background
• Ultra-sensitivity-femtogram levels detectable
• Long-lasting signals-up to 5 days
• Results in less than 3 hours
• Permanent photographic image
仅供科研使用。不可用于诊断程序。
规格
交叉反应性山羊
数量1 kit
反应性山羊
运输条件湿冰
底物类型AP(碱性磷酸酶)底物
检测方法化学发光
膜兼容性硝酸纤维素、PVDF
产品线WesternBreeze™
产品类型Western 印迹试剂盒
Unit Size1 kit
内容与储存
WesternBreeze™ 化学发光试剂盒包括封闭溶液、一抗稀释液、即用型二抗溶液(抗小鼠、抗兔或抗山羊)、即用型化学发光底物、洗涤液和孵育盘、预切割滤纸、用于膜上形成均匀的底物显影的聚酯片。每个试剂盒含有用于 20 次印迹的全套试剂。试剂盒储存于 +4°C 下。妥善储存时,可保证稳定储存 6 个月。

常见问题解答 (FAQ)

WesternBreeze化学发光检测试剂盒中的二抗溶液是否可以作为独立产品购买?

AP连接的山羊抗鼠和山羊抗兔二抗溶液可作为独立产品(货号WP20006和WP20007)购买,但是,AP连接的兔抗山羊二抗溶液不可作为独立产品购买。

WesternBreeze化学发光检测试剂盒中的封闭液/稀释液和抗体洗涤液是否可以作为独立产品购买?

可以,您可使用以下货号单独购买这些产品:

•货号WB7001(封闭液/稀释液A)
•货号WB7002(封闭液/稀释液B)
•货号WB7050(封闭液/稀释液A & B组合装)
•货号WB7003(抗体洗涤液)

WesternBreeze化学发光检测试剂盒中的化学发光底物和化学发光底物增强剂是否可以作为独立产品购买?

可以,您可使用以下货号单独购买这些产品:

•化学发光底物,货号WP20002
•化学发光底物增强剂,货号WP20003

我应该如何制备用于WesternBreeze化学发光检测的膜?

对于蛋白质免疫印迹,将蛋白质从SDS-PAGE凝胶转印到硝化纤维素或PVDF膜上后,立即使用20 mL纯水洗膜2次,每次5分钟,从而除去部分凝胶和转移缓冲液成分以及弱结合蛋白质。随后,膜可立即用于WesternBreeze化学发光免疫检测实验。
或者,将洗过的膜放在一张干净的滤纸上,在微热气流或红外灯下蒸干。适当干燥的膜可在4℃的密封容器内保存7天,保存时间取决于抗原。经水洗和干燥的硝化纤维素膜可立即用于WesternBreeze化学发光免疫检测实验方案。但是,经水洗和干燥的PVDF膜需要在甲醇中再润湿,随后用20 mL水洗涤2次,每次5分钟,最后用于WesternBreeze化学发光免疫检测实验。
对于非变性PAGE蛋白质免疫印迹,建议在所有洗涤步骤前实施干燥步骤,改善蛋白质与膜的结合。干燥后,应使用20 mL水将硝化纤维素膜洗涤2次,每次5分钟,然后再用于WesternBreeze化学发光免疫检测实验方案。干燥的PVDF膜需要在甲醇中再润湿,随后用20 mL水洗涤2次,每次5分钟,最后用于WesternBreeze化学发光免疫检测实验。

Why is the actual band size on a western blot different from the predicted size of the protein?

Western blotting is based on the separation of proteins by their size on a gel. However, migration of proteins through the gel matrix is also affected by other factors, which may cause the observed band size to be different from the predicted size.

Common causes are:
-Post-translational modification; for example phosphorylation and glycosylation increase the size of the protein
-Post-translation cleavage; many proteins are synthesized as precursor proteins, and then cleaved to give the active form
-Multimers, for example dimerization of a protein. This is usually prevented under reducing conditions, although strong interactions can result in the appearance of higher bands
-Splice variants; alternative splicing may result in different sized proteins being produced from the same gene
-Relative charge; the composition of amino acids (charged vs. non-charged)

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.