ElectroMAX™ DH10B Cells
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ElectroMAX™ DH10B Cells
Invitrogen™

ElectroMAX™ DH10B Cells

ElectroMAX DH10B Cells are electrocompetent E. coli cells offering the highest transformation efficiencies of >1 x 1010 cfu/μg plasmid DNA.자세히 알아보기
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카탈로그 번호수량
182900155 x 100 μL
카탈로그 번호 18290015
제품 가격(KRW)
517,000
Online offer
Ends: 31-Dec-2025
574,000
할인액 57,000 (10%)
Each
카트에 추가하기
수량:
5 x 100 μL
제품 가격(KRW)
517,000
Online offer
Ends: 31-Dec-2025
574,000
할인액 57,000 (10%)
Each
카트에 추가하기

ElectroMAX DH10B Cells are electrocompetent E. coli cells offering the highest transformation efficiencies of >1 x 1010 cfu/μg plasmid DNA. The high transformation efficiencies make these cells ideal for cloning both prokaryotic and eukaryotic genomic DNA and efficient plasmid rescue from eukaryotic genomes.

ElectroMAX DH10B Cells are suitable for construction of gene banks, generation of cDNA libraries using plasmid-derrived vectors, and for situations when DNA is limited. They are ideal for applications requiring high transformation efficiencies, such as with cDNA or gDNA library construction.

ElectroMAX DH10B Cells provide:
• High-efficiency transformation to maximize clones
• Enhanced genetic markers for cDNA or gDNA cloning capabilities

ElectroMAX DH10B Cell features
• Φ80lacZΔM15 marker that provides α-complementation of the β-galactosidase gene allowing blue/white screening on agar plates containing X-gal or Bluo-gal
mcrA genotypic marker and mcrBC, mrr deletion that allow cloning DNA that contains methylcytosine and methyladenine
endA1 mutation that enables increased plasmid yield and quantity

Genotype
F-mcrA Δ(mrr-hsdRMS-mcrBC) Φ80lacZΔM15 ΔlacX74 recA1 endA1 araD139Δ(ara, leu)7697 galU galK λ-rpsL nupG
Get more detailed information about specific Genotypes and Genetic Markers of our E. coli Competent Cells.

Find the strain and format that you need
DH10B cells are available in both electrocompetent and chemically competent formats.
ElectroMax DH10B T1R Cells and MegaX DH10B T1R Electrocomp Cells offer the benefit of T1 and T5 phage resistance.

Note: A high-voltage electroporation apparatus capable of generating field strengths of 16 kV/cm is required.

For Research Use Only. Not for use in diagnostic procedures.
사양
항생제 내성 박테리아Yes (Streptomycin)
블루/화이트 스크리닝Yes (lacZΔM15)
메틸화 DNA 클로닝Yes (mcrA)
불안정 DNA 클로닝Not suitable for cloning unstable DNA
에프에피솜 포함No
고처리량 호환성Low
플라스미드 품질 개선Yes (endA1)
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
E. coli (K12)
Unit SizeEach
구성 및 보관
• ElectroMAX DH10B Cells (5 x 100 μL)
Store Competent Cells at –80°C.

• pUC19 DNA (50 μL at 10 pg/μL)
Store pUC19 DNA at –20°C.

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

인용 및 참조 문헌 (9)

인용 및 참조 문헌
Abstract
Biosensor detection systems: engineering stable, high-affinity bioreceptors by yeast surface display.
Authors:Richman SA, Kranz DM, Stone JD,
Journal:Methods Mol Biol
PubMed ID:19159105
'Over the past two decades, the field of biosensors has been developing fast, portable, and convenient detection tools for various molecules of interest, both biological and environmental. Although much attention is paid to the transduction portion of the sensor, the actual bioreceptor that binds the ligand is equally critical. Tight, ... More
Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice.
Authors: Matesic L E; Yip R; Reuss A E; Swing D A; O'Sullivan T N; Fletcher C F; Copeland N G; Jenkins N A;
Journal:Proc Natl Acad Sci U S A
PubMed ID:11504925
'The d, ash, and ln coat color mutations provide a unique model system for the study of vesicle transport in mammals. All three mutant loci encode genes that are required for the polarized transport of melanosomes, the specialized, pigment-containing organelles of melanocytes, to the neighboring keratinocytes and eventually into coat ... More
Association of syncoilin and desmin: linking intermediate filament proteins to the dystrophin-associated protein complex.
Authors: Poon Ellen; Howman Emily V; Newey Sarah E; Davies Kay E;
Journal:J Biol Chem
PubMed ID:11694502
'We recently identified a novel protein called syncoilin, a putative intermediate filament protein that interacts with alpha-dystrobrevin, a member of the dystrophin-associated protein complex. Syncoilin is found at the neuromuscular junction, sarcolemma, and Z-lines and is thought to be important for muscle fiber integrity. Based on the similar protein structure ... More
Identification of diverse nerve growth factor-regulated genes by serial analysis of gene expression (SAGE) profiling.
Authors:Angelastro JM, Klimaschewski L, Tang S, Vitolo OV, Weissman TA, Donlin LT, Shelanski ML, Greene LA
Journal:Proc Natl Acad Sci U S A
PubMed ID:10984536
'Neurotrophic factors such as nerve growth factor (NGF) promote a wide variety of responses in neurons, including differentiation, survival, plasticity, and repair. Such actions often require changes in gene expression. To identify the regulated genes and thereby to more fully understand the NGF mechanism, we carried out serial analysis of ... More
Altering the substrate specificity of cephalosporin acylase by directed evolution of the Beta -subunit.
Authors: Otten Linda G; Sio Charles F; Vrielink Johanna; Cool Robbert H; Quax Wim J;
Journal:J Biol Chem
PubMed ID:12198140
'Using directed evolution, we have selected an adipyl acylase enzyme that can be used for a one-step bioconversion of adipyl-7-aminodesacetoxycephalosporanic acid (adipyl-7-ADCA) to 7-ADCA, an important compound for the synthesis of semisynthetic cephalosporins. The starting point for the directed evolution was the glutaryl acylase from Pseudomonas SY-77. The gene fragment ... More