抗体小量纯化试剂盒
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货号
CY-18110
类型
蛋白纯化
规格
10T
品牌
中科晨宇


填料为原装的GE!!国产的价格!!

抗体小量纯化试剂盒,来源于金黄色葡萄球菌的蛋白A与抗体的不变区有多个结合位点。将蛋白A与Sepharose共价交联制备的层析介质,可以用于抗体纯化。抗体与蛋白A在高盐高pH值条件下结合,在低盐pH值条件下解离。不同来源的抗体与蛋白A的结合能力有较大差异,结合与解离的条件也有区别。


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抗体小量纯化试剂盒

Antibody Purification Mini Kit

中科晨宇

CY-18110

10T

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Protein A对不同来源IgG结合剂量


高亲和性(如兔)

低亲和性(如小鼠)

Protein A Sepharose 4 FF结合剂量

35 mg/ml

3-10 mg/ml

Protein A Sepharose 4 FF每次用量

40微升

40微升50%悬液)

每次纯化抗体数量

700微克

60-200微克


一般高滴度抗血清中IgG浓度


小鼠

兔抗血清

IgG浓度

10 mg/ml

5 mg/ml

20 mg/ml


Mini kit               

PRE-EQUILIBRATION

1.Equilibrate the Spin Column with0.6mL Binding Buffer A by centrifuging the spin column at 500 × g for1minutes.

NOTE: If using one spin column, ensure that the spin column is counterbalanced with a unit of equal weight (adjusted

with distilled water).

CLARIFICATION OF SAMPLE

2.Pre-filter the sample (e.g., tissue culture supernatant, serum or ascites) through a 0.22 μmSyringeFilter toremoveany debris immediately before loading the sample.Protein precipitation is common during storage and when repeatedfreeze/thaw cycles in ascites, sera and tissue culture supernatants occur. Newly formed aggregates and precipitatingprotein complexes can foul theProteinA media and result in significantly slower flow rates. Ensure that thesamples are filteredimmediatelybefore loading, using filters with pore sizes no greater than 0.22 μm. It is critical tothe optimal performance of these devices that these instructions are rigorously followed.

SAMPLE LOADING

3.Dilute the filtered sample 1:1 v/v in Binding Buffer A. (For example, add 1 mL filtered sample to 1 mL buffer.) Pipettethe0.6mL sample into the spin column. Centrifuge the spin column at 100–150 × g for1minutes.Ideal

sample loadingconditions are obtained using a flow rate of less than 1 mL/min. It may be necessary to increase the spin time or spinspeed if any sample remainsincolumn. Alternatively, a flow rate slower than expected is indicative

of a partiallyclogged plug resulting from incomplete filtration of the sample.

WASHING

4.Wash the spin column to remove unbound contaminants by adding0.6mL Binding Buffer A and centrifuging the spincolumn for1minutes at 500 × g. Add another0.6mL Binding Buffer A and centrifuge for2more minutes at 500 × g.Theunbound wash will contain non-immunoglobulin components. A flow rate slower than expected is indicative of apartially clogged plug resulting from incomplete filtration of the sample. In the unlikely event that flow rates are

significantly slower than those expected, increase the centrifugal speed to 1000 × g with2minute spin time bursts.

ELUTION

For purifying mouse IgG1, rat IgG1, rat IgG2a, rat IgG2b and bovine IgG1 (or if you are unsure which IgG subclass youare purifying), use both elution steps 5 and 6 for your initial kit use in order to establish the mildest elution conditionpossible for the antibody. Analyze the two fractions in separate tubes to avoid sample dilution.

For purifying mouse IgG2a, mouse IgG2b, mouse IgG3, rat IgG2c, human IgG1-IgG4, rabbit IgG, guinea pig IgG1,

guinea pig IgG2, bovine IgG2 and any other IgGs, proceed to elution step 6 only.

A flow rate slower than expected is indicative of a partially clogged plug resulting from incomplete filtration of the

sample. In the unlikely event that flow rates are significantly slower than those expected, increase the centrifugal speedto 1000 × g with2minute spin time bursts.

5.Elute the bound IgG with0.1mL Elution Buffer B1 directly into a fresh centrifuge tube containing 0.005 mL NeutralizationBuffer C to bring the sample to neutral pH. Centrifuge the spin column for 5 minutes at 500 × g.Save the sample for analysis

6.Elute the bound IgG with0.1mL Elution Buffer B2 directly into a fresh centrifuge tube containing0.013 mL NeutralizationBuffer C to bring the sample to neutral pH. Centrifuge the spin column for 5 minutes at 500 × g.Save the sample for analysis.

REGENERATION

7.Wash the media with0.6mL Elution Buffer B2 by centrifuging the spin column at 500 × g for2minutes.

Re-equilibrate themedia with0.6mL of Binding Buffer A by centrifuging the spin column at 500 × g for 2 minutes.

DESALTING AND CONCENTRATING

8.If necessary, desalt and concentrate the antibody preparation using the Ultra centrifugal filter device with30,000 NMWL. Add 0.05-0.5% w/v sodium azide if the antibodies are to be stored at 2–8 °C.

We recommend freezing the antibodies in small aliquots in 50% glycerol at -20 °C for long term storage.