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pT106 [D10S2140, UTR-9747, pUC8(EcoRI)/pT106]
pT106 [D10S2140, UTR-9747, pUC8(EcoRI)/pT106]
規(guī)格:
貨期:
編號(hào):B221853
品牌:Mingzhoubio

標(biāo)準(zhǔn)菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱(chēng) pT106 [D10S2140, UTR-9747, pUC8(EcoRI)/pT106]
商品貨號(hào) B221853
Designations pT106 [D10S2140, UTR-9747, pUC8(EcoRI)/pT106]
GenBank Number

M11722

Species Homo sapiens, human
Depositors Henry M. Jackson Foundation, FJ Bollum, Henry M. Jackson Foundation
Vector
Construct size (kb): 3.700000047683716
Insert
DNA: cDNA
Insert lengths(kb): 0.9660000205039978
Tissue: lymphoblast KM-3 cell line
Gene product: terminal deoxynucleotidyl transferase [TDT]
Insert Size (kb) 0.966
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
Restriction digests of the clone give the following sizes (kb): EcoRI--2.7, 1.0; BamHI--3.4, 0.4; XmnI--1.9, 1.35, 0.5.
The insert contains the following restriction sites (approximate kb from the 5' end): BamHI--0.33; XmnI--0.5, 0.96.
Corresponds to nt 1-966 of the published sequence, including part of the coding region (nt 329-2068).
References

Peterson RC, et al. Molecular cloning of human terminal deoxynucleotidyltransferase. Proc. Natl. Acad. Sci. USA 81: 4363-4367, 1984. PubMed: 6087320

Peterson RC, et al. Expression of human terminal deoxynucleotidyl transferase in Escherichia coli. J. Biol. Chem. 260: 10495-10502, 1985. PubMed: 2863268

Bollum FJ, et al. Recombinant DNA molecules for producing terminal transferase-like polypeptides. US Patent 5,037,756 dated Aug 6 1991

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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