Recombinant Alkali-resistant Protein A Sepharose FF
| 【Numbering】BK-NRPB06L | 【CAS】CAS | ||
| 【Item No.】BK-NRPB06L-100 | 【specification】 | ||
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Product Name: Alkali-resistant Protein A Sepharose FF
English name: Alkali-tolerant Protein A NUPharose Fast Flow, rat-PA NUPharose FF
Specifications: 20 ml, 100 ml, 1 L, 1 ml pre-packed column, 5 ml pre-packed column, special specifications customized
Transportation: 2 ~ 25℃, normal pressure, avoid light
Storage: 20% ethanol, 2 ~ 8℃
Shelf life: 3 years
Related introduction:
Compared with ordinary protein A agarose gel, Alkali-resistant Protein A Sepharose FF mainly improves the alkali resistance of the gel. It can be washed with 0.1 ~ 0.5 M NaOH solution and remove the heat source. The extended carbon arms and directional binding sites are respectively designed on the bond between the skeleton and the recombinant alkali-resistant protein A to ensure the directional and firm bonding of the recombinant alkali-resistant protein A to the backbone and the high-efficiency affinity with the antibody.
Technical index:
Matrix
4% highly cross-linked agarose gel
Ligand
Recombinant Alkali Tolerant Protein A
Ligand Density
≥6 mg/ml
Filler particle size
60 ~ 180 μm
Maximum flow rate
800 cm/h
Recommended flow rate
20 ~ 100 cm/h
Working (cleaning) pH
3 ~ 11 (2 ~ 13)
Back pressure resistant
0.3 MPa
Capacity
≥40 mg/ml IgG
Features:
1) Ligand shedding: about 1~7 ng rat-PA/mg IgG, the matching rat-PA kit (NRPB53S) detects the residual rat-PA content in the eluate for multiple uses
2) Alkali resistance
Under the condition of 25℃, immerse rat-PA in different concentrations of NaOH solution:
The loading capacity of 0.1 M treatment for 72 h is maintained above 90%;
More than 80% in 0.5 M treatment for 16 h, and more than 50% in 36 h treatment;
1.0 M treatment was more than 90% for 4 h, and more than 50% for 8 h.
Picture 39.jpg
3) Acid resistance
Under the condition of 25℃, immerse rat-PA in acid solutions of different pH:
The capacity of pH 3.0, pH 2.0, 0.1 M HCl (pH 1.0) is maintained above 90% for 6 days
0.5 M HCl treatment is more than 80% for 2 days, and more than 50% for 6 days
Picture 40.jpg
4) Pressure resistance
Instrument: AKTA explorer 100
Pillar: 1.0 cm×30 cm
Flow rate: increase by 0.5 ml/min every 30 s
Picture 41.jpg
5) Service life
The IgG in bovine serum was purified for 200 cycles, and treated with 0.1 M NaOH for 15 minutes each time. No significant load loss was found after 200 uses.
Picture 1.png
Application examples:
Binding buffer: 20 mM phosphate buffer, 150 mM NaCl, pH 7.4
Elution buffer: 0.1 M citrate buffer, pH 4.0
Neutralization buffer: 1 M Tris-HCl, pH 9.0
1) 1 ml Alkali-resistant Protein A Sepharose FF pre-packed column is washed with 5-10 column volumes of distilled water to remove the preservation solution;
2) Equilibrate 5-10 bed volumes with binding buffer and buffer;
3) Dilute 5 ml of rabbit polyantiserum to 50 ml with binding buffer, filter and load the sample with a 0.45 μm filter;
4) Wash with binding buffer for another 5-10 bed volumes;
5) Elute the antibody with elution buffer, collect the elution peak, and adjust its pH to neutral with neutralization buffer;
6) Regenerate and clean with 3 ~ 5 column bed volumes of 0.1 M NaOH solution after each use;
7) The purity of the rabbit polyclonal antibody eluted by SDS-PAGE (Figure 1) electrophoresis analysis is above 95%.
Picture 2.png
figure 1
Precautions:
1) The pre-packed column is easy to use and can complete the purification task without equipment.
2) After the sample is eluted, the pH is generally very low, so you should immediately neutralize the collected antibody solution to neutral with an alkaline neutralization buffer (such as 1 M Tris-HCl, pH 9.0), or put it in a collection container beforehand. 5% ~ 20%, pH 7 ~ 9 buffer (such as 1 M Tris-HCl or 1 M phosphate buffer) to help maintain the biological activity of the antibody and avoid antibody inactivation.
3) When using, ensure that the temperature of the column and the buffer are the same to avoid bubbles in the column bed. If bubbles have already occurred, you can repack the column by yourself.
4) In-place cleaning should be performed after use. Generally, it is recommended to clean 1 to 3 column volumes (10 to 30 min) with 0.1 M NaOH, and immediately use equilibration buffer to clean more than 5 column volumes.
5) For in-place cleaning with higher requirements (disinfection, removal of endotoxin, ultra-fast protein residues, etc.), you can first clean with a balance buffer containing a reducing agent (such as 100 mM DTT, β-ME or 1-mercaptoglycerol) 3 ~ 5 column volumes, then wash 1 ~ 5 column volumes (10 ~ 30 min) with 0.1 ~ 0.5 M NaOH, and then wash more than 5 column volumes with sterile endotoxin-free equilibration buffer.
6) Although this product has good alkali resistance, long-term use of higher NaOH concentration (such as 0.5 mol/L) for cleaning will still shorten the service life. It is recommended to clean with 0.1 M NaOH every 1 to 3 times. Wash with 0.5 M NaOH every 5 to 20 times.
7) In order to better protect the packing, strong pH changes should be avoided. It is recommended that after acidic elution of the target antibody, it should be restored to neutral with an equilibration buffer, and then washed with NaOH.
8) This product has a very low ligand shedding rate (<10 ng/mg IgG), combined with alkali resistance, and is especially suitable for the production of monoclonal antibodies. However, experiments have found that the first use of the ligand after long-term storage will have a higher shedding rate. It is recommended that for the first use after long-term storage, first wash 3 to 5 column volumes with an acidic eluent, and then equilibrate and purify the sample with an equilibration buffer.
Recommended flow rate
Prepacked column volume 1 ml 5 ml 10 ml
Flow rate (ml /min) 0.2 1 2
9)
Recommended flow rate
Prepacked column volume
1 ml
5 ml
10 ml
Flow rate (ml /min)
0.2
1
2
Message
English name: Alkali-tolerant Protein A NUPharose Fast Flow, rat-PA NUPharose FF
Specifications: 20 ml, 100 ml, 1 L, 1 ml pre-packed column, 5 ml pre-packed column, special specifications customized
Transportation: 2 ~ 25℃, normal pressure, avoid light
Storage: 20% ethanol, 2 ~ 8℃
Shelf life: 3 years
Related introduction:
Compared with ordinary protein A agarose gel, Alkali-resistant Protein A Sepharose FF mainly improves the alkali resistance of the gel. It can be washed with 0.1 ~ 0.5 M NaOH solution and remove the heat source. The extended carbon arms and directional binding sites are respectively designed on the bond between the skeleton and the recombinant alkali-resistant protein A to ensure the directional and firm bonding of the recombinant alkali-resistant protein A to the backbone and the high-efficiency affinity with the antibody.
Technical index:
Matrix
4% highly cross-linked agarose gel
Ligand
Recombinant Alkali Tolerant Protein A
Ligand Density
≥6 mg/ml
Filler particle size
60 ~ 180 μm
Maximum flow rate
800 cm/h
Recommended flow rate
20 ~ 100 cm/h
Working (cleaning) pH
3 ~ 11 (2 ~ 13)
Back pressure resistant
0.3 MPa
Capacity
≥40 mg/ml IgG
Features:
1) Ligand shedding: about 1~7 ng rat-PA/mg IgG, the matching rat-PA kit (NRPB53S) detects the residual rat-PA content in the eluate for multiple uses
2) Alkali resistance
Under the condition of 25℃, immerse rat-PA in different concentrations of NaOH solution:
The loading capacity of 0.1 M treatment for 72 h is maintained above 90%;
More than 80% in 0.5 M treatment for 16 h, and more than 50% in 36 h treatment;
1.0 M treatment was more than 90% for 4 h, and more than 50% for 8 h.
Picture 39.jpg
3) Acid resistance
Under the condition of 25℃, immerse rat-PA in acid solutions of different pH:
The capacity of pH 3.0, pH 2.0, 0.1 M HCl (pH 1.0) is maintained above 90% for 6 days
0.5 M HCl treatment is more than 80% for 2 days, and more than 50% for 6 days
Picture 40.jpg
4) Pressure resistance
Instrument: AKTA explorer 100
Pillar: 1.0 cm×30 cm
Flow rate: increase by 0.5 ml/min every 30 s
Picture 41.jpg
5) Service life
The IgG in bovine serum was purified for 200 cycles, and treated with 0.1 M NaOH for 15 minutes each time. No significant load loss was found after 200 uses.
Picture 1.png
Application examples:
Binding buffer: 20 mM phosphate buffer, 150 mM NaCl, pH 7.4
Elution buffer: 0.1 M citrate buffer, pH 4.0
Neutralization buffer: 1 M Tris-HCl, pH 9.0
1) 1 ml Alkali-resistant Protein A Sepharose FF pre-packed column is washed with 5-10 column volumes of distilled water to remove the preservation solution;
2) Equilibrate 5-10 bed volumes with binding buffer and buffer;
3) Dilute 5 ml of rabbit polyantiserum to 50 ml with binding buffer, filter and load the sample with a 0.45 μm filter;
4) Wash with binding buffer for another 5-10 bed volumes;
5) Elute the antibody with elution buffer, collect the elution peak, and adjust its pH to neutral with neutralization buffer;
6) Regenerate and clean with 3 ~ 5 column bed volumes of 0.1 M NaOH solution after each use;
7) The purity of the rabbit polyclonal antibody eluted by SDS-PAGE (Figure 1) electrophoresis analysis is above 95%.
Picture 2.png
figure 1
Precautions:
1) The pre-packed column is easy to use and can complete the purification task without equipment.
2) After the sample is eluted, the pH is generally very low, so you should immediately neutralize the collected antibody solution to neutral with an alkaline neutralization buffer (such as 1 M Tris-HCl, pH 9.0), or put it in a collection container beforehand. 5% ~ 20%, pH 7 ~ 9 buffer (such as 1 M Tris-HCl or 1 M phosphate buffer) to help maintain the biological activity of the antibody and avoid antibody inactivation.
3) When using, ensure that the temperature of the column and the buffer are the same to avoid bubbles in the column bed. If bubbles have already occurred, you can repack the column by yourself.
4) In-place cleaning should be performed after use. Generally, it is recommended to clean 1 to 3 column volumes (10 to 30 min) with 0.1 M NaOH, and immediately use equilibration buffer to clean more than 5 column volumes.
5) For in-place cleaning with higher requirements (disinfection, removal of endotoxin, ultra-fast protein residues, etc.), you can first clean with a balance buffer containing a reducing agent (such as 100 mM DTT, β-ME or 1-mercaptoglycerol) 3 ~ 5 column volumes, then wash 1 ~ 5 column volumes (10 ~ 30 min) with 0.1 ~ 0.5 M NaOH, and then wash more than 5 column volumes with sterile endotoxin-free equilibration buffer.
6) Although this product has good alkali resistance, long-term use of higher NaOH concentration (such as 0.5 mol/L) for cleaning will still shorten the service life. It is recommended to clean with 0.1 M NaOH every 1 to 3 times. Wash with 0.5 M NaOH every 5 to 20 times.
7) In order to better protect the packing, strong pH changes should be avoided. It is recommended that after acidic elution of the target antibody, it should be restored to neutral with an equilibration buffer, and then washed with NaOH.
8) This product has a very low ligand shedding rate (<10 ng/mg IgG), combined with alkali resistance, and is especially suitable for the production of monoclonal antibodies. However, experiments have found that the first use of the ligand after long-term storage will have a higher shedding rate. It is recommended that for the first use after long-term storage, first wash 3 to 5 column volumes with an acidic eluent, and then equilibrate and purify the sample with an equilibration buffer.
Recommended flow rate
Prepacked column volume 1 ml 5 ml 10 ml
Flow rate (ml /min) 0.2 1 2
9)
Recommended flow rate
Prepacked column volume
1 ml
5 ml
10 ml
Flow rate (ml /min)
0.2
1
2
| Warm tips: Suzhou Beike nano products are only used for scientific research, not for human body,different batches of products have different specifications and performance |
Message
|
| Warm tips: Suzhou Beike nano products are only used for scientific research, not for human body,different batches of products have different specifications and performance.The website pictures are from the Internet. The pictures are for reference only. Please take the real object as the standard. In case of infringement, please contact us to delete them immediately. |
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