pCDM8-ICAM-1-载体及构建-试剂-生物在线
Biovector Co.,LTD
pCDM8-ICAM-1

pCDM8-ICAM-1

商家询价

产品名称: pCDM8-ICAM-1

英文名称: pCDM8-ICAM-1 质粒图谱序列抗性说明书价格报价

产品编号: BiovectorPCDM8

产品价格: 0

产品产地: Biovector Inc. USA

品牌商标: Biovector, Addgene, ATCC, Invi

更新时间: null

使用范围: null

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Product Information

Order ID

Name

Description

BiovectorPCDM8

pCDM8-ICAM-1

pCDM8-ICAM-1. in E.coli, AmpR,TetR. Storage:4

Backbone vector

Gene/insert name:ICAM-1 H. sapiens (human)

Insert size:1800

Alt name:CD54

Alt name:pCD1.8

GenBank ID:NM_000201

ICAM-1 Cloning site 5:XbaI

ICAM-1 Cloning site 3:XbaI

The host strain is MC1061/P3 and the bacteria should be cultured in 12.5ug/mL ampicillin and 16ug/mL tetracycline. (supF)

Recovery

1. Obtain an LB agar plate with the appropriate antibiotic.

2. Using a sterile pipette tip, touch the bacteria growing within the punctured area of the stab culture. (A sterilized wire loop or sterile toothpick can be used in place of a sterile pipette tip.)

3. Run this tip lightly over a section of the plate, as shown in the figure, to create streak #1.

4. Using another sterile pipette tip, pass through streak #1 and spread the bacteria over a second section of the plate, to create streak #2.

5. Using a third sterile pipette tip, pass through streak #2 and spread the bacteria over the last section of the plate, to create streak #3.

6. Grow overnight in a 37 PoP C incubator (unless a different growth temperature is indicated on the plasmid datasheet).

7. In the morning, single colonies should be visible. If the bacterial growth is too dense, re-streak onto a new agar plate to obtain single colonies.

载体信息:

Plasmid Type:

Mammalian Expression

Promotor:

CMV

Cloning Method:

Unknown

Size:

4356

5 Sequencing 1 Primer:

T7

Notes:

Start of the nucleotide sequence between the Eco-pMB1 ori and the SV40 ori. pCDM8 is a shuttle vector designed for high-level transient expression of cloned cDNA in mammalian cells. The protein encoded by the cDNA can be expressed under control of the human cytomegalovirus immediate early promoter (CMV-IE) with enhancer and the SV40 polyadenylation site. The T7 promoter is used for in vitro transcription of the cDNA insert. The small HIV (human immunodeficiency virus) fragment (29 nucleotides) between the CMV and T7 promoter sequences has an enhancer function. The presence of the polyoma and SV40 origins of replication enables the vector to replicate episomally in mammalian cells expressing large T-antigen (e.g. WOB, COS cells). The supF tRNA suppressor gene is used for selection in E. coli (MC1061[p3]). The M13 origin is useful for synthesis of single-stranded DNA upon infection with the M13 helper phage. The SspI fragment (153 bp) of the 3' UTR region of the SV40 small t-antigen is missing, but without effect on the function of the vector.

Stable:

Unspecified

Constitutive:

Constitutive

Viral/Non-Viral:

Nonviral

载体序列:

1     ggcgtaatct  gctgcttgca   aacaaaaaaa ccaccgctac  cagcggtggt 50

51   ttgtttgccg    gatcaagagc taccaactct   ttttccgaag   gtaactggct  100

101  tcagcagagc gcagatacca  aatactgtcc   ttctagtgta    gccgtagtta  150

151  ggccaccact  tcaagaactc  tgtagcaccg  cctacatacc   tcgctctgct    200

201  aatcctgtta   ccagtggctg  ctgccagtgg  cgataagtcg  tgtcttaccg   250

251  ggttggactc  aagacgatag ttaccggata   aggcgcagcg gtcgggctga 300

301  acggggggtt cgtgcacaga gcccagcttg  gagcgaacga cctacaccga  350

351  actgagatac  ctacagcgtg  agcattgaga  aagcgccacg cttcccgaag  400

401  ggagaaaggc      ggacaggtat ccggtaagcg gcagggtcgg aacaggagag      450

451  cgcacgaggg agcttccagg  gggaaacgcc tgctatcttt     atgatcctgt   500

501  cgggtttcgc  cacctctgac   ttgagcgtcg  atttttgtga    tgctcgtcag   550

551  gggggcggag     cctatggaaa  aacgccagca acgcaagcta  gcttctagct   600

601  agaaattgta  aacgttaata   ttttgttaaa    attcgcgtta   aatttttgtt     650

651  aaatcagctc  attttttaac     caataggccg aaatcggcaa aatcccttat    700

701  aaatcaaaag aatagcccga  gatagggttg  agtgttgttc   cagtttggaa  750

751  caagagtcca  ctattaaaga   acgtggactc  caacgtcaaa  gggcgaaaaa      800

801  ccgtctatca   gggcgatggc cgcccactac  gtgaaccatc  acccaaatca  850

851  agttttttgg    ggtcgaggtg ccgtaaagca  ctaaatcgga  accctaaagg  900

901  gagcccccga tttagagctt    gacggggaaa      gccggcgaac gtggcgagaa 950

951  aggaagggaa     gaaagcgaaa ggagcgggcg     ctagggcgct  ggcaagtgta 1000

1001      gcggtcacgc tgcgcgtaac  caccacaccc  gccgcgctta  atgcgccgct  1050

1051      acagggcgcg tactatggtt    gctttgacga  gaccgtataa  cgtgctttcc    1100

1101      tcgttggaat   cagagcggga      gctaaacagg aggccgatta  aagggatttt   1150

1151      agacaggaac ggtacgccag ctggattacc   gcggtctttc   tcaacgtaac  1200

1201      actttacagc   ggcgcgtcat  ttgatatgat   gcgccccgct  tcccgataag  1250

1251      ggagcaggcc agtaaaagca ttacccgtgg   tggggttccc  gagcggccaa 1300

1301      agggagcaga      ctctaaatct    gccgtcatcg  acttcgaagg  ttcgaatcct    1350

1351      tcccccacca   ccatcacttt    caaaagtccg  aaagaatctg  ctccctgctt    1400

1401      gtgtgttgga  ggtcgctgag tagtgcgcga  gtaaaattta   agctacaaca  1450

1451      aggcaaggct tgaccgacaa  ttgcatgaag  aatctgctta   gggttaggcg 1500

1501      ttttgcgctg    cttcgcgatg   tacgggccag atatacgcgt   tgacattgat   1550

1551      tattgactag   ttattaatag    taatcaatta   cggggtcatt  agttcatagc   1600

1601      ccatatatgg   agttccgcgt   tacataactt    acggtaaatg  gcccgcctgg  1650

1651      ctgaccgccc  aacgaccccc  gcccattgac  gtcaataatg  acgtatgttc   1700

1701      ccatagtaac  gccaataggg actttccatt    gacgtcaatg  ggtggactat  1750

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