다음 MAP메이트™는 통합될 수 없습니다: -다른 분석 완충용액이 필요한 MAP메이트™. -인산 특이성 및 총 MAP메이트™ 조합, 예: 총 GSK3β 및 GSK3β(Ser 9). -PanTyr 및 자리 특이성 MAP메이트™, 예: Phospho-EGF 수용체 및 phospho-STAT1(Tyr701). -단일 표적(Akt, STAT3)를 위한 1개 이상의 1 phospho-MAP메이트™. - GAPDH 및 β-Tubulin은 panTyr를 포함하는 키트 또는 MAP메이트™와 통합될 수 없습니다.
Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
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List
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96-Well Plate
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다른 시약 추가 (MAP메이트 사용을 위해 완충용액과 검출 키트가 필요함)
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48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
공간 절약 옵션 다수의 키트를 구매하시는 고객은 고용량 저장을 위해 키트 포장을 제거하고 비닐백에 담긴 멀티플레스 분석 구성품을 받아 저장 공간을 절약하도록 선택할 수 있습니다.
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이제 다른 키트를 사용자 지정하거나, 사전 혼합된 키트를 선택하거나, 결재하거나 또는 주문 도구를 종료할 수 있습니다.
Ultrapure water is used for many steps of blotting: sample, buffer, gels and rinsing solutions preparation. Prior to blotting itself, either for Southern or Northern blotting, the sample preparation implies a particular care of water quality used to protect raw material (respectively DNA or RNA).
The major sample preparation steps are the isolation by extraction, amplification and a pretreatment to denature RNA to prevent formation of base-paired secondary structure.
Water Quality Parameters
Ions Charged molecules can interfere during migration electrophoresis steps by changing the global charge of the solutions (buffer, sample…) and then either accelerating or delaying the migration.
The concentration of ions is also important during the hybridization step. In order to carry on the hybridization in optimum conditions, specific concentrations should be respected. Starting with water virtually free of ions (resistivity 18.2 MΩ•cm @ 25°C) ensures the preparation of the buffers at the right ionic strength and pH.
Organics Organic molecules can create interferences in the hybridization process. Those molecules that are negatively charged can behave just as the DNA and RNA and bind non-specifically in place of the DNA or RNA. Positively charged molecules can actually bind to the DNA or RNA and the oligonucleotides, retarding or interfering with the hybridization process. Consequently, low TOC value (< 10 ppb or µg/L) is recommended to ensure good water quality in terms of organic content.
Nucleases Nucleases degrade the NA samples. These enzymes are efficiently removed using ultrafiltration. The ultrafilter is installed at the outlet of the purification unit, just before water is drawn from the system and used. Please refer to the section on nuclease-free water.
Bacteria Bacteria liberate nucleases that degrade Nucleic Acids samples. They contain DNA, which can interfere with DNA to be checked. Finally, they release ions and organics that can have a negative effect on blotting steps Water purified with an Ultrafilter (BioPak) has bacteria levels < 0.1 cfu/mL.
In summary, considering the overall processes associated with the blotting steps, water should be nuclease-free and bacteria-free, have a high resistivity and a low TOC. All this can be obtained using an ultrafiltration device at the point-of-use (the outlet) of a water purification unit delivering high purity water. Please refer to the following sections for more information: Nuclease-free water, gel electrophoresis, PCR and DNA Sequencing.