pET-33b(+)載體基本信息
別名: | pET33b, pET 33b |
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質粒類型: | 大腸桿菌蛋白表達 |
表達水平: | 高 |
克隆方法: | 多克隆位點,限制性內切酶 |
載體大小: | 5383 bp |
5' 測序引物: | T7 |
5' 測序引物序列: | T7: 5'-TAATACGACTCACTATAGGG-3' |
載體標簽: | His (中間和C端), N-Thrombin |
載體抗性: | Kanamycin |
備注: |
Production of target proteins suitable for site-specific 32P-labeling; Nterm thrombin cleavage site; Nterm enterokinase cleavage site
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產品目錄號: | 69054-3 |
穩定性: | 瞬時表達 Transient |
組成型: | 組成型 Constitutive |
病毒/非病毒: | 非病毒 |
Feature Name | Start | End | |
---|---|---|---|
T7_terminator | 129 | 1 | |
T7_Terminal_primer | 69 | 87 | |
T7_leader | 238 | 206 | |
Xpress_fwd_primer | 239 | 221 | |
T7_transl_en_RBS | 337 | 321 | |
lacO | 382 | 355 | |
T7_promoter | 400 | 382 | |
tet (300 - 563) | 432 | 695 | |
pBRrevBam_primer | 503 | 484 | |
lacI | 778 | 1869 | |
tet (576 - 851) | 1928 | 2203 | |
ROP | 2678 | 2869 | |
pGEX_3_primer | 2885 | 2863 | |
pBR322_origin | 3903 | 3284 | |
KanR2 | 4009 | 4824 |
ORF | Start | End | |
---|---|---|---|
ORF frame 3 | 537 | 1037 | |
ORF frame 1 | 910 | 1869 | |
ORF frame 1 | 4009 | 4824 |
Enzyme Name | Cut |
---|---|
XhoI | 158 |
NotI | 166 |
EagI | 166 |
HindIII | 173 |
SalI | 179 |
SacI | 190 |
EcoRI | 192 |
BamHI | 198 |
NheI | 230 |
NdeI | 237 |
NcoI | 310 |
XbaI | 349 |
BglII | 415 |
BclI | 1151 |
ApaI | 1348 |
EcoRV | 1587 |
HpaI | 1643 |
FspI | 2219 |
NruI | 4097 |
ClaI | 4131 |
XmaI | 4312 |
SmaI | 4314 |
The pET-33b(+) vector (Cat. No. 69054-3) is derived from pET-28b(+) and carries a 15bp sequence encoding the protein kinase A (PKA) site RRASV, located between the thrombin cleavage and Nde I sites (1). Proteins expressed in pET-33b(+) can be easily purified by metal chelation chromatography (via either N- or C-terminal His?Tag® sequences) and efficiently labeled with 32P- or 33P-gATP and the catalytic subunit of cAMP-dependent protein kinase from heart muscle. Labeled proteins can be used as direct probes in protein-protein interaction studies. 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 T7 terminator primer (Cat. No. 69337-3).