宁波泰斯拓生物

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浙江省宁波市镇海区庄市街道兴庄路9号创e慧谷42号楼B幢401室
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pBM2240

货号 TS166038
中文名称 null
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产品简介
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产品名称: pBM2240
商品货号: TS166038
Designations: pBM2240
Depositors: M Johnston
Biosafety Level: 1
Vector Information:
Size (kb): 7.2500000000000000
Vector: pBM2240 (phagemid)
Construction: pRS316, lambdaMG3
Marker(s):URA3,ampR
Construct size (kb): 7.25
Features: marker(s): ampR, URA3
replicon: pMB1, CEN6/ARS4
centromere: CEN6
Applications:
shuttle vector
vector for other uses
Comments:
Restriction digests of the clone give the following sizes (kb): EcoRI/XhoI--7.3; KpnI--5.6, 1.5; BamHI/XbaI--6.4, 0.9.
S. cerevisiae is cotransformed with the lambda clone of interest and vector linearized with an EcoRI/XhoI double digest. Ura+ colonies are tested for complementation of a mutant phenotype.
YC-type shuttle vector designed to clone yeast genes that are difficult to clone by rescuing inserts from the vector lambdaMG3 by homologous recombination.
Constructed by insertion of a 0.858 kb BamHI-XbaI fragment and a 1.5 kb KpnI fragment from lambdaMG3 into the corresponding sites of pRS316 (ATCC 77145).
The order of the major features in this plasmid is: f1 ori - lacZ - T7 promoter - KpnI/lambdaMG3/KpnI - MCS - BamHI/lambdaMG3/XbaI - T3 promoter - pMB1 ori - ampR - CEN6/ARS4 - URA3.
Media: ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Growth Conditions:
Temperature: 37.0°C
References:

Erickson JR, Johnston M. Direct cloning of yeast genes from an ordered set of lambda clones in Saccharomyces cerevisiae by recombination in vivo. Genetics 134: 151-157, 1993. PubMed: 8514124

Shipped: freeze-dried