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產(chǎn)品名稱(chēng):丁酰*酯酶
M0136 丁酰*酯酶/BCHE/BUCHE BR,4u/mg 500u sigma分裝 1500 1050 9001-8-5 2~8℃
1.2KU sigma分裝 3200 2240
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SD6031 5xProtein Loading Buffer (no reducing buffer) 5ml
SD6032 5xProtein Loading Buffer (no deturation buffer) 5ml
SD6035 10XTris-Glycine Gel Running Buffer(no deturation buffer)pH8.8緩沖液 500ml
SD6036 IEF anode Buffer 50xsolution :proteomics grade pH 2..4緩沖液 50ml
SD6037 IEF cathnode Buffer 10xsolution: proteomics grade pH 10.0緩沖液 50ml
SD6038 IEF Sample Buffer 4 X solution: proteomics grade pH 10.0 10ml
SD6040 Zymogram Development Buffer [10X] (0.5M Tris.HCL, 2M NaCl, 50mM CaCl2, 0.2% Brij®-35, pH 7.5) 緩沖液 500ml
SD6042 MOPS Running Buffer [10X] (200mM MOPS (pH 7.0), 80mM Sodium acetate, 10mM EDTA)緩沖液 1L
SD6043 MOPS Running Buffer [10X] (200mM MOPS (pH 7.0) 80mM Sodium acetate, 10mM EDTA)緩沖液 1gallon
SD6045 Blue Native PAGE Elecrtophoresis Running Buffer (Anode buffer 500ml + Cathode buffer 500ml) Anode buffer (50 mM Bis-Tris pH 7.0) Cathode buffer (50 mM Tricine 15 mM Bi-Tris 0.02% Coomassie blue G pH 7.0)緩沖液 1L
SD6046 (2x)TBE-Urea Sample Buffer (178m M tris-HCl pH 8.0 , 178m M boric acid,4 m M EDTA,7 M Urea,24% ficoll,0.02% bromophenol blue,0.04% xylene cyanole FF) 5ml
SD6047 (2x)Tricine Sample Buffer (400m M Tris-HCl p H 6.8, ,4% SDS,80% Glycerol,0.08% CBB-G250) 5ml
SD6049 (2x)Zymogram Sample Buffer (125m M Tris.HCL, pH 6.8,50% Glycerol,8%SDS, 0.02% bromophenol blue) 1ml
SD6050 Discontinuous Buffer System (425ml Anode buffer + 500ml Cathode buffer ,Anode buffer (200m M Tris-HCL,, p H 8.9) Cathode buffer (100m M Tris,,100m M Tricine ,0.1% SDS, p H 8.3)緩沖液 1L
SD6051 [20X]MOPS/ SDS Running Buffer (MOPS 1M,Tris 1M,SDS 2%,EDTA 20.m M p H 7.7,) 緩沖液 500ml
SD6052 [20X]MES /SDS Running buffer (MES 1M,Tris 1M,SDS 2%,EDTA 20.m M ,p H 7.3 ) 緩沖液 100ml
SD6055 (2x)Blue Native PAGE Sample Buffer 1.5M 6- aminocaproic acid, 100 mM bisTris-HCI, 2.% Tritonx-100, and 0.7% Coomassie blue G pH 7.0 20% glycerol 5ml
SD8104 TBS buffer with non-fat powdered milk 緩沖液 1pk
SD8113 TBS buffer with BSA 緩沖液 1pk
SD8319 2xProtein Gel Loading Dye 2x蛋白質(zhì)加樣緩沖液 1ml
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實(shí)驗(yàn)過(guò)程:質(zhì)粒質(zhì)量檢測(cè)
將抽提好的核酸直接用于后續(xù)的實(shí)驗(yàn),是*可靠的檢測(cè)方法;除此之外的檢測(cè)方法,都是相對(duì)的, 而且并不十分可信。目前用于正式實(shí)驗(yàn)前檢測(cè)核酸質(zhì)量的方法,一是電泳,二是紫外分光光度儀。電泳檢測(cè)的主要是核酸的完整性和大小,只要核酸不是太小或者太 大 (超出電泳分離范圍),該方法還是非??尚诺?;電泳還可以用于估計(jì)核酸的濃度,但其準(zhǔn)確度與經(jīng)驗(yàn)有關(guān);另外,電泳也可能提供某些雜質(zhì)污染的信息,但是同樣 與經(jīng)驗(yàn)有關(guān)。紫外分光光度儀檢測(cè)的是純度和核酸含量,然而,由于紫外分光光度儀不能確保非常準(zhǔn)確,而該儀器的靈敏度又非常高,所以,提供的結(jié)果并不十分可 信。一般講,同時(shí)進(jìn)行紫外和電泳檢測(cè),綜合二者的結(jié)果,可以做出一個(gè)更合理的判斷。但由于這兩個(gè)方法都有缺陷,所以,即使出現(xiàn)壞的結(jié)果能用于后續(xù)實(shí)驗(yàn)而好 的結(jié)果卻不能用于后續(xù)實(shí)驗(yàn),也不用大驚小怪。
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