pGB29-质粒载体-ATCC-DSM-CCUG-泰斯拓生物

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pGB29
pGB29
规格:
货期:
编号:TS165870
品牌:Testobio
产品名称: pGB29
商品货号: TS165870
Designations: pGB29
GenBank Number:

J05411

Species: Elizabethkingia miricola
Depositors: Genzyme Corp., G Barsomian, Genzyme Corp.
Applications:
produces protein peptide-N(4)-(N-acetyl-beta-D-glucosaminyl) asparagine amidase F
Vector:
Construct size (kb): 6.200
Insert:
DNA: genomic
Insert lengths(kb): 3.30
Gene product: peptide-N(4)-(N-acetyl-beta-D-glucosaminyl) asparagine amidase F ngl
Target Gene: peptide-N(4)-(N-acetyl-beta-D-glucosaminyl) asparagine amidase F
Insert Size (kb): 3.300
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.

Shipping Information:

Shipped: xa0Freeze dried E. coli containing the phagemid.

Comments:
Restriction digests of the clone give the following sizes (kb): BamHI--uncut; Sau3AI--1.0, 0.7, 0.6, + smaller; BglII--3.5, 3.2.
The sequenced portion of the insert contains the following restriction sites (approximate kb from the 5 end): EcoRV--1.33; HindIII--0.80; NdeI--0.85; PvuII--0.93; EcoRI--1.6. Additional EcoRI sites are known to occur beyond the site indicated.
Contains the complete coding sequence (nt 139-1203). A subclone deleting EcoRI fragments downstream of the gene was used for sequencing and expression studies.
Proteins of 35, 37 and 38 kDa are expressed. Expression is independent of orientation in the vector, suggesting the presence of an endogenous promoter that functions in E. coli.
The vector was constructed from pBluescript SK+ by converting ApaI and SacI sites into BglII sites.
The insert in this clone was isolated from ATCC 33958, Elizabethkingia miricola, formerly Flavobacterium meningosepticum.
References:

Barsomian GD, et al. Cloning and expression of peptide-N(4)-(N-acetyl-beta-D-glucosaminyl) asparagine amidase F in Escherichia coli. J. Biol. Chem. 265: 6967-6972, 1990. PubMed: 2182635

Barsomian GD, et al. Endo F-free PNGase. US Patent 5,238,821 dated Aug 24 1993

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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pGB29

  • 货号: TS165870
  • 好评
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  • 品牌 : TESTOBIO
产品名称: pGB29
商品货号: TS165870
Designations: pGB29
GenBank Number:

J05411

Species: Elizabethkingia miricola
Depositors: Genzyme Corp., G Barsomian, Genzyme Corp.
Applications:
produces protein peptide-N(4)-(N-acetyl-beta-D-glucosaminyl) asparagine amidase F
Vector:
Construct size (kb): 6.200
Insert:
DNA: genomic
Insert lengths(kb): 3.30
Gene product: peptide-N(4)-(N-acetyl-beta-D-glucosaminyl) asparagine amidase F ngl
Target Gene: peptide-N(4)-(N-acetyl-beta-D-glucosaminyl) asparagine amidase F
Insert Size (kb): 3.300
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.

Shipping Information:

Shipped: xa0Freeze dried E. coli containing the phagemid.

Comments:
Restriction digests of the clone give the following sizes (kb): BamHI--uncut; Sau3AI--1.0, 0.7, 0.6, + smaller; BglII--3.5, 3.2.
The sequenced portion of the insert contains the following restriction sites (approximate kb from the 5 end): EcoRV--1.33; HindIII--0.80; NdeI--0.85; PvuII--0.93; EcoRI--1.6. Additional EcoRI sites are known to occur beyond the site indicated.
Contains the complete coding sequence (nt 139-1203). A subclone deleting EcoRI fragments downstream of the gene was used for sequencing and expression studies.
Proteins of 35, 37 and 38 kDa are expressed. Expression is independent of orientation in the vector, suggesting the presence of an endogenous promoter that functions in E. coli.
The vector was constructed from pBluescript SK+ by converting ApaI and SacI sites into BglII sites.
The insert in this clone was isolated from ATCC 33958, Elizabethkingia miricola, formerly Flavobacterium meningosepticum.
References:

Barsomian GD, et al. Cloning and expression of peptide-N(4)-(N-acetyl-beta-D-glucosaminyl) asparagine amidase F in Escherichia coli. J. Biol. Chem. 265: 6967-6972, 1990. PubMed: 2182635

Barsomian GD, et al. Endo F-free PNGase. US Patent 5,238,821 dated Aug 24 1993

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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