ElectroMAX™ DH12S Cells
본 제품은 LMO 제품으로, 고객 분께서 LMO 신고 시스템을 통해 직접 수입 신고를 진행해주셔야 합니다. 자세히보기
ElectroMAX™ DH12S Cells
Invitrogen™

ElectroMAX™ DH12S Cells

ElectroMAX DH12S Cells, a derivative of DH10B cells, are suitable for transformation by electroporation. They may be used for production자세히 알아보기
Have Questions?
카탈로그 번호수량
183120175 x 100 μL
카탈로그 번호 18312017
제품 가격(KRW)
482,000
Online offer
Ends: 31-Dec-2025
566,000
할인액 84,000 (15%)
Each
카트에 추가하기
수량:
5 x 100 μL
제품 가격(KRW)
482,000
Online offer
Ends: 31-Dec-2025
566,000
할인액 84,000 (15%)
Each
카트에 추가하기

ElectroMAX DH12S Cells, a derivative of DH10B cells, are suitable for transformation by electroporation. They may be used for production of single-stranded (ss)DNA and in procedures requiring high transformation efficiencies, such as generation of cDNA, genomic, and subtractive cDNA libraries.

Benefits of ElectroMAS DH12S Competent Cells
• Maximize yield of transformants using small amounts of DNA
• High-yield plasmid production
• Ability to create representative genomic libraries

Optimized strain for ssDNA production
The DH12S strain is endA+, which allows the production of ssDNA with less contamination of double-stranded (ds)DNA. The lacIq on the F´ episome allows for regulatable expression from the lac promoter. Most E. coli strains used in cloning genomic DNA have intact the systems that restrict DNA containing methylated cytosine and adenine residues (coded by mcrA, mcrB, mcrC, and mrr genes). Such wild type systems have been eliminated in the DH12S strain, allowing the construction of more representative genomic libraries and use in more efficient plasmid rescue procedures. M13KO7 helper phage is supplied for the production of ssDNA and together with DH12S cells is utilized in antibody discovery workflows (e.g., screening Ab libraries using panning method).

ElectroMAX DH12S Cells offer:
• >1 x 1010 transformants/μg efficiency with electroporation for unsurpassed cloning results
• A unique genotype to support production of exceptionally clean single stranded DNA
• Stable F´ episome to eliminate the need for growth on minimal media
• Better sequence representation eliminating mcrA, mcrBC, mrr, hsdRMS restriction systems
• Blue/white screening of recombinant clones due to lacZΔM15
• Ready-to-use M13KO7 helper phage for single stranded DNA production

Note: A High-voltage electroporation apparatus is required.

Genotype
φ80ΔlacZΔM15 mcrA Δ(mrr-hsdRMS-mcrBC) araD139 Δ(ara-leu)7697 Δ(lacX74 galU galK rpsL(StrR) nupG recA1 / F′ [proAB+lacIqZΔM15 Tn10(TetR)]

Genetic marker descriptions

Find the strain and format that fits your needs
DH10B Cells, the parent strain of DH12S, are available in both electrocompetent and chemically competent formats.
MAX Efficiency DH5αF´IQ Competent Cells may be used for ssDNA production and come with M13mp18 RF DNA control and are chemically competent cells.

For Research Use Only. Not for use in diagnostic procedures.
사양
항생제 내성 박테리아Yes (Streptamycin, Tetracycline)
블루/화이트 스크리닝Yes (lacZΔM15)
메틸화 DNA 클로닝Yes (mcrA)
불안정 DNA 클로닝Not suitable for cloning unstable DNA
에프에피솜 포함Yes
고처리량 호환성Low
플라스미드 품질 개선No
플라스미드May be used for plasmids >20 kb
비메틸화 DNA 준비No
제품라인ElectroMAX
제품 유형Electrocompetent Cells
수량5 x 100 μL
재조합 감소Yes (recA1)
배송 조건Dry Ice
T1 Phage - 저항성(tonA)No
형질전환 효율 수준High Efficiency (>1 x 109 cfu/μg)
형식Tube
프로모터Laclq
E. coli (K12)
Unit SizeEach
구성 및 보관
• ElectroMAX DH12S Cells (5 x 100 μL)
• pUC19 DNA (50 μL at 10 pg/μL)
• M13KO7 Helper Phage (2 x 1 mL)
Store at –80°C.

• S.O.C. Medium (2 x 6 mL)
Store S.O.C. Medium at 4°C or room temperature.

자주 묻는 질문(FAQ)

Can a single-stranded DNA be generated using M13 helper phage?

Yes. Use a strain that expresses endonuclease A (e.g., DH12S, DH11S). The orientation of the single-stranded DNA will be the opposite of that generated by Gene II and Exo III.

Can encapsulated phagemid DNA or M13 phage be used to infect bacteria?

Single-stranded DNA viral particles like M13 require the presence of an F pilus in order to infect E. coli. This criterion is met by TOP10F', DH5? F'IQ, INV?F', Stbl4, OmniMAX2-T1 and DH12S cells. These cells are not traD mutants, which effectively allows the cells to retain the F' episome. Transforming single-stranded DNA can cause a 100- to 1,000-fold reduction in efficiency compared to viral particles.