Yes, Tris buffers should work.
P6611
HIS-Select® Nickel Affinity Gel
(1:1 suspension in a 20% ethanol solution)
동의어(들):
Ni-NTA resin, nickel charged agarose
크기 선택
₩280,039
크기 선택
About This Item
₩280,039
추천 제품
결합
magnetic beads
Quality Level
양식
(1:1 suspension in a 20% ethanol solution)
특징
hydrophilic
포장
pkg of 1 mL
pkg of 100 mL
pkg of 25 mL
pkg of 5 mL
pkg of 500 mL
농도
1.5-2.4 mL/mL (suspension in packed gel)
기술
protein purification: suitable
색상
faint blue to very dark blue
Matrix
6% Beaded Agarose
용량
>15 mg/mL, gel binding capacity (protein)(with an approx. 30 kDa protein)
전이 온도
flash point 32 °C (closed cup)
저장 온도
2-8°C
일반 설명
애플리케이션
특징 및 장점
- High selectivity for higher purity.
- Unique non-charged hydrophilic linkage reduces non-specific binding.
- Binding capacity for histidine-tagged protein is greater than 15 mg/mL.
- Binding under denaturing or non-denaturing conditions.
- One-step purification.
- Minimizes unwanted ionic interactions.
- Minimal nickel leaching.
- Bead size: 45-165 μm.
결합
물리적 형태
저장 및 안정성
법적 정보
관련 제품
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
89.6 °F - closed cup
Flash Point (°C)
32 °C - closed cup
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
관련 콘텐츠
Protein purification techniques, reagents, and protocols for purifying recombinant proteins using methods including, ion-exchange, size-exclusion, and protein affinity chromatography.
이온교환, 크기 배제 및 단백질 친화성 크로마토그래피를 포함한 방법을 사용하는 재조합형 단백질 정제를 위한 단백질 정제 기법, 시약 및 프로토콜.
단백질 발현 기술은 연구, 치료제, 백신 생산을 지원하는 다양한 발현 시스템에 사용됩니다.
Protein expression technologies for various expression systems supporting research, therapeutics, and vaccine production.
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Can Tris buffers be used instead of phosphate buffer for HIS-Select® Nickel Affinity Gel, Product P6611?
1 답변-
도움이 되었습니까?
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Can imidazole be used with HIS-Select® Nickel Affinity Gel, Product P6611?
1 답변-
For column chromatography, no more than 20 mM is suggested in the extract, equilibration, and wash buffers to prevent non-specific binding of proteins. No more than 250 mM is suggested for the elution buffers. Many proteins will elute with imidazole levels as low as 100 to 200 mM. For batch methods the imidazole concentration may have to be reduced or eliminated.When a protein is expressed at low levels, the presence of the imidazole limits the binding of the protein in the batch method but not when used in a column.
도움이 되었습니까?
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What is the Department of Transportation shipping information for this product?
1 답변-
Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.
도움이 되었습니까?
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What needs to be done if the HIS-Select® Nickel Affinity Gel, Product P6611, resin turns brown on reuse?
1 답변-
During purification many protein extracts tend to discolor an affinity gel during the loading step. The original color will return after the wash or elution step. If the color is still not changing strip and recharge the affinity gel with nickel. Wash with EDTA and recharge with Nickel solution.
도움이 되었습니까?
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Can I use SDS with HIS-Select® Nickel Affinity Gel, Product P6611?
1 답변-
0.1% SDS has been used with some samples, with no adverse effects on the observed protein binding. However, SDS will effectively coat proteins and may block the binding to the column. It is probably very protein-specific and an SDS concentration that works for one protein may not work for another.
도움이 되었습니까?
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Why won't my recombinant protein with a histidine-containing tag bind to HIS-Select® Nickel Affinity Gel, Product P6611?
1 답변-
Verify the pH and composition of sample and equilibration buffers. Make sure there are no chelating or reducing agents present in the extraction buffer. If using the batch mode, remove imidazole. Run the affinity purification under denaturing conditions. Run a Western blot of the extract to verify that the recombinant protein is present.
도움이 되었습니까?
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