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pGC24 plasmid in E. coli
pGC24 plasmid in E. coli
规格:
货期:
编号:TS214883
品牌:Testobio
产品名称: pGC24 plasmid in E. coli
商品货号: TS214883
Designations: pGC24 plasmid in E. coli
Species: Aspergillus awamori Nakazawa
Depositors: Cetus Corp., A Belt, Cetus Corp.
Applications:
produces protein glucoamylase
Vector:
Construct size (kb): 6.55
DESCRIPTION OF VECTOR COMPONENT:
Name of vector: pTRP3
Intact vector size: 4.460
Type of vector: plasmid
Vector end: HindIII
Vector end: HindIII
Cloning sites: HindIII
Polylinker sites:
Other unique sites: BamHI
Construction: pVH153, pBR322
Host range: Escherichia coli
Features (with orientation and position when available):
promoter: trp, ->
ribosome-binding site: , ->
restriction site: HindIII, ->
marker(s): tetR, ->
replicon: pMB1
marker(s): ampR, Cross references:
Insert:
DNA: cDNA
DESCRIPTION OF INSERT COMPONENT:
Genome: Aspergillus awamori
Gene name: glucoamylase
Contains complete coding sequence?: U
Strain: NRRL 15271
Type of DNA: cDNA
Insert end: HindIII
Insert end: HindIII
Insert size (kb): 2.11
Cross references:
Insert lengths(kb): 2.10
Gene product: glucoamylase
Target Gene: glucoamylase
Insert Size (kb): 2.110
Media: ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Biosafety Level: 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Comments:
Insert contains internal PstI and BamHI sites.
Restriction digests of the clone give the following sizes (kb): HindIII--4.5, 2.4; PstI--5.2, 1.9; BamHI--5.8, 1.1.
Expresses the gene product under the control of the Escherichia coli trp promoter.
The vector was constructed by inserting an EcoRI/ClaI fragment with Escherichia coli trp promoter and RBS into pBR322. A HindIII fragment of about 2.2 kb containing the gene with poly(A) signal was cloned into the HindIII site.
References:

Nunberg J, et al. Glucoamylase cDNA. US Patent 4,794,175 dated Dec 27 1988

Disclosure: This material is cited in a US or other Patent and may not be used to infringe the claims. Depending on the wishes of the Depositor, ATCC may be required to inform the Patent Depositor of the party to which the material was furnished. This material may not have been produced or characterized by ATCC.
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pGC24 plasmid in E. coli

  • 货号: TS214883
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  • 品牌 : TESTOBIO
产品名称: pGC24 plasmid in E. coli
商品货号: TS214883
Designations: pGC24 plasmid in E. coli
Species: Aspergillus awamori Nakazawa
Depositors: Cetus Corp., A Belt, Cetus Corp.
Applications:
produces protein glucoamylase
Vector:
Construct size (kb): 6.55
DESCRIPTION OF VECTOR COMPONENT:
Name of vector: pTRP3
Intact vector size: 4.460
Type of vector: plasmid
Vector end: HindIII
Vector end: HindIII
Cloning sites: HindIII
Polylinker sites:
Other unique sites: BamHI
Construction: pVH153, pBR322
Host range: Escherichia coli
Features (with orientation and position when available):
promoter: trp, ->
ribosome-binding site: , ->
restriction site: HindIII, ->
marker(s): tetR, ->
replicon: pMB1
marker(s): ampR, Cross references:
Insert:
DNA: cDNA
DESCRIPTION OF INSERT COMPONENT:
Genome: Aspergillus awamori
Gene name: glucoamylase
Contains complete coding sequence?: U
Strain: NRRL 15271
Type of DNA: cDNA
Insert end: HindIII
Insert end: HindIII
Insert size (kb): 2.11
Cross references:
Insert lengths(kb): 2.10
Gene product: glucoamylase
Target Gene: glucoamylase
Insert Size (kb): 2.110
Media: ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Biosafety Level: 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Comments:
Insert contains internal PstI and BamHI sites.
Restriction digests of the clone give the following sizes (kb): HindIII--4.5, 2.4; PstI--5.2, 1.9; BamHI--5.8, 1.1.
Expresses the gene product under the control of the Escherichia coli trp promoter.
The vector was constructed by inserting an EcoRI/ClaI fragment with Escherichia coli trp promoter and RBS into pBR322. A HindIII fragment of about 2.2 kb containing the gene with poly(A) signal was cloned into the HindIII site.
References:

Nunberg J, et al. Glucoamylase cDNA. US Patent 4,794,175 dated Dec 27 1988

Disclosure: This material is cited in a US or other Patent and may not be used to infringe the claims. Depending on the wishes of the Depositor, ATCC may be required to inform the Patent Depositor of the party to which the material was furnished. This material may not have been produced or characterized by ATCC.
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