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pET-44c(+)图谱序列抗性价格Biovector质粒库

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pET44c载体基本信息

出品公司:别名:质粒类型:表达水平:克隆方法:载体大小:5' 测序引物:5' 测序引物序列:  3' 测序引物:3' 测序引物序列:  载体标签:载体抗性:备注:产品目录号:稳定性:组成型:病毒/非病毒:
EMD Biosciences (Novagen)
pET44c, pET 44c
大肠杆菌蛋白表达
多克隆位点,限制性内切酶
7309 bp
T7
T7: 5'-TAATACGACTCACTATAGGG-3'
ColiDOWN
ColiDOWN: 5'-TTCACTTCTGAGTTCGGCATG-3'
C-HSV, N-His, C-His, N-Thrombin, N-Nus, N-EK
Ampicillin
Both Nterm and Cterm His tags; Nterm thrombin cleavage site; Nterm enterokinase cleavage site; a,b,c vary by MCS.
71124-3
瞬时表达 Transient
组成型 Constitutive
非病毒

pET44c载体质粒图谱和多克隆位点信息

pet44c载体图谱
pet44c多克隆位点

Feature Name
Start
End
 
T7_Terminal_primer6987
rrnB_T2_terminator168141
rrnB_T1_terminator343300
rrnB_terminator466309
EK693679
S15789745
6xHIS23402323
T7_transl_en_RBS23772361
lacO24222395
T7_promoter24402422
tet (300 - 563)24762739
pBRrevBam_primer25472528
lacI28223913
ROP44854676
pGEX_3_primer46924670
pBR322_origin57105091
AmpR_promoter57975825
Ampicillin58686728
ORF
Start
End
 
ORF frame 14272130
ORF frame 22352499
ORF frame 123233081
ORF frame 229543913
ORF frame 358686728
Enzyme Name
Cut
PacI503
XhoI530
PmlI576
NotI592
EagI592
HindIII599
KpnI624
SalI626
PstI639
AscI641
EcoRI654
BamHI660
SacI672
SmaI719
XmaI717
SacII795
SpeI826
BglII941
MscI1073
StuI1126
NcoI1401
NdeI2351
XbaI2389
ApaI3392
HpaI3687
FspI6432

pET44c载体简介

The pET-44 vectors are designed for cloning and high-level expression of peptide sequences fused with the 495 aa Nus•Tag™ protein. Compared to the pET-43.1 series, the pET-44 vectors encode an additional N-terminal His•Tag. Unique sites are shown on the circle map. Note that the sequence is numbered by the pBR322 convention, so the T7 expression region is reversed on the circle map. The cloning/expression region of the coding strand transcribed by T7 RNA polymerase is shown below. The f1 origin is oriented so that infection with helper phage will produce virions containing single stranded DNA that corresponds to the coding strand. Therefore, single stranded sequencing should be performed using the COLIDOWN primer (Cat. No. 70845-3). Vector encoded sequence can be completely removed when cloning into the PshA I or Sma I sites (as shown below) by cleaving the Nus•Tag fusion protein with enterokinase or thrombin, respectively.

pET44c载体序列

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