Western及IP细胞裂解液
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产品编号 P0013
数量
¥ 189.00
产品包装:
100ml
产品简介
使用说明
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Western及IP细胞裂解液(Cell lysis buffer for Western and IP),是一种在非变性条件下裂解细胞或组织样品从而制备蛋白样品的裂解液。本裂解液裂解的细胞或组织样品,可以用于PAGE,Western,免疫沉淀(immunol precipitation,IP)、免疫共沉淀(co-IP)和ELISA等。
本产品可以用于动物、植物的细胞或组织样品,也可以用于真菌或细菌样品。
碧云天生产的不同裂解液的主要特点和差异,以及如何选择裂解液可参考我们的相关网页:
http://www.beyotime.com/support/lysis-buffer.htm

Western及IP细胞裂解液的主要成分为20mM Tris(pH7.5),150mM NaCl,1% Triton X-100,以及sodium pyrophosphate,β-glycerophosphate,EDTA,Na3VO4,leupeptin等多种抑制剂。可以有效抑制蛋白的降解,并维持原有的蛋白间相互作用。
用Western及IP细胞裂解液裂解得到的蛋白样品,可以用碧云天生产的BCA蛋白浓度测定试剂盒(P0009/P0010/P0010S/ P0011/P0012/P0012S)测定蛋白浓度。由于含有较高浓度的Triton X-100等干扰物质,不能用Bradford法测定由本裂解液裂解得到样品的蛋白浓度。
包装清单:

产品编号 产品名称 包装
P0013 Western及IP细胞裂解液 100ml
说明书 1份

保存条件:
-20℃保存,一年有效。
注意事项:
为取得最佳的使用效果,尽量避免过多的反复冻融。可以适当分装后使用。
需自备PMSF。PMSF(ST506)可以向碧云天订购。也可以选购总体效果更佳的碧云天生产的P1045/P1046 蛋白酶磷酸酶抑制剂混合物(通用型, 50X),或者根据具体用途选择P1048/P1049 蛋白酶磷酸酶抑制剂混合物(通用型, 质谱兼容, 50X)P1050/P1051蛋白酶磷酸酶抑制剂混合物(哺乳动物样品抽提用, 50X)P1055/P1056 蛋白酶磷酸酶抑制剂混合物(植物样品抽提用, 50X)P1060/P1061 蛋白酶磷酸酶抑制剂混合物(真菌或酵母抽提用, 50X)P1065/P1066 蛋白酶磷酸酶抑制剂混合物(细菌抽提用, 50X)。如果无需检测磷酸化蛋白,也可以选不含磷酸酶抑制剂的蛋白酶抑制剂化合物。
裂解样品的所有步骤都需在冰上或4℃进行。
关于裂解液的选择,一方面可以参考碧云天的相关网页:http://www.beyotime.com/support/lysis-buffer.htm 选择合适的裂解液;另一方面也需要通过一些预实验来摸索最佳的适合您实验条件的裂解液。
本产品仅限于专业人员的科学研究用,不得用于临床诊断或治疗,不得用于食品或药品,不得存放于普通住宅内。
为了您的安全和健康,请穿实验服并戴一次性手套操作。

使用说明:
1.对于培养细胞样品:
a.融解Western及IP细胞裂解液,混匀。取适当量的裂解液,在使用前数分钟内加入PMSF,使PMSF的最终浓度为1mM,或者根据实验需要加入适当的上述蛋白酶磷酸酶抑制剂混合物。
b.对于贴壁细胞:去除培养液,用PBS、生理盐水或无血清培养液洗一遍(如果血清中的蛋白没有干扰,可以不洗)。按照6孔板每孔加入100-200微升裂解液的比例加入裂解液。用枪吹打数下,使裂解液和细胞充分接触。通常裂解液接触动物细胞1-2秒后,细胞就会被裂解。植物细胞宜在冰上裂解2-10min。
对于悬浮细胞:离心收集细胞,轻轻vortex或者弹击管底以把细胞尽量分散开。按照6孔板每孔细胞加入100-200微升裂解液的比例加入裂解液。轻弹管底以充分裂解细胞。充分裂解后应没有明显的细胞沉淀。如果细胞量较多,必需分装成50-100万细胞/管,然后再裂解。大团的细胞较难裂解充分,而少量的细胞由于裂解液容易和细胞充分接触,相对比较容易裂解充分。
对于细菌或酵母:对于1ml菌液或酵母液,离心去上清,如果有必要可以使用PBS洗涤一次,充分去除液体后,轻轻vortex或者弹击管底以把细菌或酵母尽量弹散。加入100-200微升裂解液,轻轻vortex或者弹击管底以混匀,冰上裂解2-10min。如果希望获得更好的裂解效果,细菌和酵母可以分别使用溶菌酶和破壁酶(Lyticase)消化,然后再使用本裂解液进行裂解。
裂解液用量说明:通常6孔板每孔细胞或者1ml的菌液或酵母液中的细菌和酵母量加入100微升裂解液已经足够,但如果细胞密度非常高可以适当加大裂解液的用量到150微升或200微升。每100万动物细胞用100微升本产品裂解后获得的上清,其蛋白浓度约为2-4mg/ml,不同细胞有所不同。
c.充分裂解后,10000-14000g离心3-5分钟,取上清,即可进行后续的PAGE、Western、免疫沉淀和免疫共沉淀等操作。
2.对于组织样品:
a.把组织剪切成细小的碎片。
b.融解Western及IP细胞裂解液,混匀。取适当量的裂解液,在使用前数分钟内加入PMSF,使PMSF的最终浓度为1mM,或者根据实验需要加入适当的上述蛋白酶磷酸酶抑制剂混合物。
c.按照每20毫克组织加入100-200微升裂解液的比例加入裂解液。(如果裂解不充分可以适当添加更多的裂解液,如果需要高浓度的蛋白样品,可以适当减少裂解液的用量。)
d.用玻璃匀浆器匀浆,或使用碧云天生产的E6600 TissueMaster™手持式组织研磨仪研磨,直至充分裂解。也可以把组织样品冷冻后液氮研磨,研磨充分后加入裂解液进行裂解。
e.充分裂解后,10000-14000g离心3-5分钟,取上清,即可进行后续的PAGE、Western、免疫沉淀和免疫共沉淀等操作。每20mg冻存的小鼠肝脏组织用200微升本裂解液裂解后获得的上清,其蛋白浓度约为15-25mg/ml,不同状态的不同组织有所不同。
f.如果组织样品本身非常细小,可以适当剪切后直接加入裂解液裂解,通过强烈vortex使样品裂解充分。然后同样离心取上清,用于后续实验。直接裂解的优点是比较方便,不必使用匀浆器或研磨设备,缺点是不如匀浆或研磨那样裂解比较充分。

附录:碧云天生产的各种裂解液主要特点、差异和选择
首先请参考下表,了解各种裂解液的主要特点和差异。

产品编号 P0013 P0013B P0013C P0013D P0013F P0013G P0013J P0013K
产品名称 Western及IP细胞裂解液 RIPA裂解液(强) RIPA裂解液(中) RIPA裂解液(弱) NP-40裂解液 SDS裂解液 Western及IP细胞裂解液(无抑制剂) RIPA裂解液(强,无抑制剂)
有效裂解成分 1% Triton X-100 1% Triton X-100, 1% deoxycholate, 0.1% SDS 1% NP-40, 0.5% deoxycholate, 0.1% SDS 1% NP-40, 0.25% deoxycholate 1% NP-40 1% SDS 1% Triton X-100 1% Triton X-100, 1% deoxycholate, 0.1% SDS
裂解强度 温和 温和 温和 温和
对膜蛋白的提取 一般 很好 较好 一般 一般 很好 一般 很好
对胞浆蛋白的提取 很好 很好 很好 很好 很好 很好 很好 很好
对核蛋白的提取 较好 很好 较好 较好 较好 很好 较好 很好
胞浆磷酸化蛋白提取 很好 很好 很好 很好 很好 很好 很好 很好
细胞核转录因子提取 很好 很好 很好 很好 很好 很好 很好 很好
含蛋白酶抑制剂
含磷酸酯酶抑制剂
不同物种样品兼容性
主要用途 WB, IP,co-IP WB, IP WB, IP WB, IP, co-IP WB, IP,co-IP WB, ChIP WB, IP,co-IP WB, IP

用于普通的Western、IP或co-IP,我们推荐使用Western及IP细胞裂解液(P0013),该裂解液已被国内各大研究机构广泛使用,发表大量SCI论文,用户普遍反映很好。裂解细胞或组织后,没有非常粘滞的透明状DNA团块形成,不必采用超声处理等就可以非常理想地用于后续操作。另外该裂解液裂解的产物也适合用于磷酸化蛋白的Western检测。
对于某些特殊蛋白的IP,如果发现Western及IP细胞裂解液(P0013)效果不是非常理想,可以尝试用RIPA裂解液(强、中或弱)或NP-40裂解液。如果发现IP的时候背景很高,即非特异的蛋白也被IP下来,则需要选用裂解强度较高的裂解液,例如RIPA裂解液(强或中)。如果发现目的蛋白无法被IP下来,则说明裂解液的强度过强,可以使用较为温和的裂解液例如RIPA裂解液(弱)或NP-40裂解液。
对于某些难溶解蛋白的Western,如果发现Western及IP细胞裂解液(P0013)效果不是非常理想,可以尝试使用裂解强度更高的裂解液例如RIPA裂解液(强、中)或SDS裂解液。使用RIPA裂解液(强)的用户也非常多,发表了大量SCI论文。
用于特定用途需要自行添加特定抑制剂或不需要添加抑制剂时,可以考虑选购P0013JP0013KP0013J在很多时候可以兼容酶活性和生物小分子的检测,对于特定的酶或生物小分子的检测是否兼容需 要自行测试,碧云天不提供具体的应用信息。P0013J的裂解能力比P0013K弱一些,但用于酶活性和生物小分子时,P0013J的兼容性通常会更好一些。

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Neurosci Lett 2010;469(2):278-82. (IF 2.274)
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Acta Pharmacol Sin 2010;31(6):679-86. (IF 5.064)
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Eur J Pharmacol 2010;641(2-3):199-206. (IF 3.263)
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Life Sci 2010;87(7-8):254-60. (IF 3.647)
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J Surg Res 2010 Jun 1;161(1):119-25. (IF 1.841)
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Mol Biol Rep 2010 Oct;37(7):3193-8. (IF 1.402)
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J NEUROSCI METH 2010 Nov 30;193(2):226-31. (IF 2.214)
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J GEN VIROL l. 2010 Dec;91(Pt 12):2907-17. (IF 3.376)
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EXP TOXICOL PATHOL 2011 Jan;63(1-2):69-78. (IF 2.023)
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Micron 2011 Jan;42(1):17-28. (IF 1.726)
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PLoS One 2011 Apr 15;6(4):e18618. (IF 2.74)
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J Cell Physiol 2011 May;226(5):1176-85. (IF 5.546)
82. Wang W, Chen X, Li X, Wang L, Zhang H, He Y, Wang J, Zhao Y, Zhang B, Xu Y.
Reproduction 2011 May;141(5):643-51. (IF 3.206)
83. Liu C, Shi Y, Li H, Wang Y, Yang K.
Horm Metab Res 2011 Jun;43(6):391-6. (IF 2.562)
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Toxicol In Vitro 2011 Jun;25(4):882-9. (IF 2.959)
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J EXP CLIN CANC RES 2011 Sep 16;30:83. (IF 7.068)
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Parasitology 2011 Sep;138(10):1259-71. (IF 2.783)
87. Tang DQ, Wei YQ, Yin XX, Lu Q, Hao HH, Zhai YP, Wang JY, Ren J.
Fitoterapia 2011 Sep;82(6):920-6. (IF 2.527)
88. Sun YL, Ping ZG, Li CJ, Sun YF, Yi KL, Chen L, Li XY, Wang XL, Zhou X.
Reprod Domest Anim 2011 Oct;46(5):889-95. (IF 1.641)
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Int Immunopharmacol 2011 Nov;11(11):1871-6. (IF 3.943)
90. Tang DQ, Wei YQ, Gao YY, Yin XX, Yang DZ, Mou J, Jiang XL.
Phytother Res 2011 Nov;25(11):1640-7. (IF 4.087)
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Eur J Pharmacol 2011 Nov 1;669(1-3):76-83. (IF 3.263)
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FUND CLIN PHARMACOL 2011 Dec;25(6):700-7. (IF 2.754)
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Cancer Lett 2011 Dec 8;311(2):160-70. (IF 7.36)
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J Int Med Res 2012;40(5):1745-51. (IF 1.287)
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Mol Biol Rep 2012 Jan;39(1):493-500. (IF 1.402)
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Mol Med Rep 2012 Jan;5(1):256-9. (IF 2.1)
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Exp Cell Res 2012 Feb 15;318(4):424-34. (IF 3.383)
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Metab Brain Dis 2012 Mar;27(1):91-100. (IF 2.726)
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Molecules 2012 Mar 22;17(3):3586-98. (IF 3.267)
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Inflammation 2012 Jun;35(3):1169-78. (IF 3.212)
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J ZHEJIANG UNIV-SC B 2012 Jun;13(6):465-77. (IF 2.082)
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Apoptosis 2012 Jun;17(6):579-90. (IF 4.543)
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J Nutr Biochem 2012 Jul;23(7):716-24. (IF 4.873)
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Int Immunopharmacol 2012 Jul 23;14(2):209-216. (IF 3.943)
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Food Chem Toxicol 2012 Jul;50(7):2368-75. (IF 4.679)
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J Nutr Biochem 2012 Aug;23(8):994-1006. (IF 4.873)
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Biol Reprod 2012 Sep 7;87(3):54. (IF 3.322)
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IUBMB Life 2012 Sep;64(9):748-56. (IF 3.244)
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Virus Res 2012 Oct;169(1):1-7. (IF 2.934)
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IUBMB Life 2012 Nov;64(11):901-10. (IF 3.244)
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Oncol Rep 2012 Nov;28(5):1719-26. (IF 3.417)
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Mol Med Rep 2012 Dec;6(6):1243-8. (IF 2.1)
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CELL PHYSIOL BIOCHEM 2013;31(2-3):189-98. (IF 5.5)
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EVID-BASED COMPL ALT 2013;2013:646728. (IF 1.813)
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Int Immunopharmacol 2013 Feb;15(2):275-81. (IF 3.943)
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《中德临床肿瘤学杂志》 2013 Apr;12(4):181-187.
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J Cell Physiol 2013 May;228(5):991-1001. (IF 5.546)
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INT J BIOCHEM CELL B 2013 May;45(5):987-94. (IF 3.673)
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Medicinal Chemistry Research 2013 Jun;22(6):2855-61. (IF 1.72)
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J Surg Res 2013 Nov;185(1):300-9. (IF 1.841)
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Mol Neurobiol 2014 Feb;49(1):368-79. (IF 4.5)
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CURR CANCER DRUG TAR 2014 Feb;14(2):156-66. (IF 2.912)
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PLoS One 2014 Mar 13;9(3):e91564. (IF 2.74)
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Cell Biol Int 2014 Mar;38(3):343-54. (IF 2.571)
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BBA-BIOMEMBRANES 2014 Mar;1843(3):652-63. (IF 3.411)
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Cell Signal 2014 May;26(5):1048-59. (IF 3.968)
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INT J CLIN EXP PATHO 2014 Aug 15;7(9):5750-61. (IF 0.252)
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Biochem Pharmacol 2014 Aug 1;90(3):265-75. (IF 4.96)
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Exp Gerontol 2014 Aug;56:3-12. (IF 3.376)
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Exp Cell Res 2014 Sep 10;327(1):48-56. (IF 3.383)
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Biomed Pharmacother 2014 Oct;68(8):1031-6. (IF 4.545)
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Iran J Pharm Res 2015 Winter;14(1):251-61. (IF 1.505)
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Immunol Invest 2015;44(6):566-77. (IF 2.511)
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Biosci Trends 2015 Feb;9(1):42-8. (IF 1.553)
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Int Immunopharmacol 2015 Mar;25(1):112-20. (IF 3.943)
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BIOCHEMISTRY-MOSCOW+ 2015 Mar;80(3):379-89. (IF 1.978)
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J CANCER RES CLIN 2015 Mar;141(3):419-29. (IF 3.656)
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Cell Biol Int 2015 Apr;39(4):364-72. (IF 2.571)
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Int Immunopharmacol 2015 Jun;26(2):401-8. (IF 3.943)
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Cytokine 2015 Jul;74(1):137-44. (IF 2.952)
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Immunol Lett 2015 Jul;166(1):45-54. (IF 3.276)
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Int Immunopharmacol 2015 Sep;28(1):344-53. (IF 3.943)
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Cell Signal 2015 Oct;27(10):2026-34. (IF 3.968)
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SCI REP-UK 2015 Oct 26;5:15584. (IF 3.998)
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Cell Signal 2015 Dec;27(12):2343-54. (IF 3.968)
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FREE RADICAL BIO MED 2015 Dec;89:209-19. (IF 6.17)
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TOXICOL APPL PHARM  2015 Dec 1;289(2):231-9. (IF 3.616)
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Oxid Med Cell Longev 2016;2016:8923860. (IF 5.076)
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Curr Mol Med 2016;16(8):767-775. (IF 1.6)
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CELL PHYSIOL BIOCHEM 2016;40(1-2):146-154. (IF 5.5)
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Mol Med Rep 2016 Jan;13(1):237-42. (IF 2.1)
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J INTERF CYTOK RES 2016 Feb;36(2):129-39. (IF 2.032)
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PLoS One 2016 Feb 29;11(2):e0150324. (IF 2.74)
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SCI REP-UK 2016 Feb 18;6:21620. (IF 3.998)
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ONCOTARGET 2016 Mar 29;7(13):16282-96. (IF 5.168)
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Environ Pollut 2016 Mar;210:48-56. (IF 6.792)
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Biochem Pharmacol 2016 Mar 1;103:85-97. (IF 4.96)
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ONCOTARGET 2016 Mar 8;7(10):11284-98. (IF 5.168)
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Biol Trace Elem Res 2016 Apr;170(2):449-58. (IF 2.639)
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BIOCHEM BIOPH RES CO 2016 Apr 22;473(1):212-8. (IF 2.985)
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Mol Nutr Food Res 2016 May;60(5):1139-49. (IF 5.309)
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Toxicology 2016 May 16;357-358:52-64. (IF 4.099)
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PLoS One 2016 May 12;11(5):e0155502. (IF 2.74)
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Nutrients 2016 May 5;8(5). pii: E258. (IF 4.546)
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Mol Med Rep 2016 May;13(5):3929-35. (IF 2.1)
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J Neurochem 2016 Jun;137(5):701-13. (IF 4.066)
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Phytomedicine 2016 Jun 1;23(6):641-53. (IF 4.268)
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SCI REP-UK 2016 Jul 27;6:30406. (IF 3.998)
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Cancer Lett 2016 Jul 1;376(2):268-77. (IF 7.36)
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Apoptosis 2016 Jul;21(7):825-35. (IF 4.543)
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Biomed Pharmacother 2016 Jul;81:176-81. (IF 4.545)
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FREE RADICAL BIO MED 2016 Aug;97:179-91. (IF 6.17)
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Biochem Pharmacol 2016 Sep 1;115:94-103. (IF 4.96)
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Virus Res 2016 Sep 2;223:153-60. (IF 2.934)
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TOXICOL APPL PHARM  2016 Sep 15;307:72-80. (IF 3.616)
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FISH SHELLFISH IMMUN 2016 Sep;56:330-5. (IF 3.298)
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Gene 2016 Sep 1;589(1):12-9. (IF 2.984)
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IUBMB Life 2016 Sep;68(9):748-55. (IF 3.244)
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Mol Med Rep 2016 Oct;14(4):3413-20. (IF 2.1)
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SCI REP-UK 2016 Nov 7;6:36576. (IF 3.998)
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Cell Mol Neurobiol 2016 Nov;36(8):1389-1397. (IF 3.606)
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J Ethnopharmacol 2016 Nov 4;192:413-422. (IF 3.69)
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Mol Nutr Food Res 2016 Nov;60(11):2331-2342. (IF 5.309)
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Curr Mol Med 2017;17(2):149-159. (IF 1.6)
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BBA-BIOMEMBRANES 2017 Jan 10;1864(4):613-624. (IF 3.411)
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Biomed Pharmacother 2017 Jan;85:248-255. (IF 4.545)
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Exp Ther Med 2017 Jan;13(1):235-241. (IF 1.785)
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NEURO-ONCOLOGY 2017 Jan;131(2):255-265. (IF 10.247)
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Environ Toxicol 2017 Feb;32(2):705-716. (IF 3.118)
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Neuropharmacology 2017 Feb;113(Pt A):556-566. (IF 4.431)
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Int J Biol Macromol 2017 Mar;96:652-668. (IF 5.162)
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SCI REP-UK 2017 Mar 17;7:44744. (IF 3.998)
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Oncol Lett 2017 Mar;13(3):1348-1352. (IF 2.311)
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J Mol Neurosci 2017 Mar;61(3):351-358. (IF 2.678)
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Behav Brain Res 2017 Mar 1;320:412-419. (IF 2.977)
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Neurochem Res 2017 Apr;42(4):1211-1218. (IF 3.038)
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Oncol Lett 2017 Apr;13(4):2684-2690. (IF 2.311)
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Mol Med Rep 2017 Apr;15(4):1647-1653. (IF 2.1)
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Int J Mol Med 2017 May;39(5):1119-1126. (IF 3.098)
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Exp Ther Med 2017 May;13(5):2529-2536. (IF 1.785)
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