宁波泰斯拓生物

www.testobio.com
  • 本公司产品仅供体外研究使用,不用于临床诊断
首页  /  产品中心  /  进口菌株

产品中心

试剂盒
菌株
质粒
试剂
联系我们  CONTACT US

0574-87917803

testobio@163.com

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
最新促销

货号: TS263591

名称: Candida metapsilosis


货号: TS263592

名称: Candida sake


货号: TS131909

名称: HFBCI28


货号: TS131910

名称: Septoria passiflorae Sydow, anamorph


货号: TS131911

名称: Graphium cuneiferum (Berkeley et Broome) Mason et Ellis


货号: TS131912

名称: Streptomyces scabiei (Thaxter) Lambert and Loria


货号: TSTOA0001

名称: Marisediminicola antarctica


货号: TS276951

名称: Real Time PCR EasyTM-Taqman


货号: TS276952

名称: Bacillus subtilis


货号: TS276954

名称: Bacillus subtilis

p304

货号 TS133986
中文名称 null
适应种属
检测范围
微信小陈 微信小章
在线留言
产品简介
购买须知
产品名称: p304
商品货号: TS133986
Designations: p304
GenBank Number:

J00127

Species: Homo sapiens, human
Applications:
The depositor notes that the fibrinogen clones (ATCC 59706-59710) are suitable for applications in gene mapping or involving nucleic acid hybridization, but they are not suitable starting material for expression in mammalian cells.
Vector:
Construct size (kb): 4.400000095367432
Insert:
DNA: cDNA
Insert lengths(kb): 2.0
Tissue: liver
Gene product: fibrinogen, A alpha polypeptide FGA
Alleles: A1, A2
Insert Size (kb): 2.0
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: Distributed: DNA (dried). Rehydrate with TE. (amount: 2 ug)
Comments:
Restriction digests of the clone give the following sizes (kb): EcoRI--2.2, 1.9, 0.4; XhoI--4.8; EcoRI/XhoI--2.1, 1.1, 0.98; PstI--3.3, 1.1; BglI--3.2, 1.2; EcoRI/HindIII--2.3, 1.9; NcoI--2.5, 1.9.
Insert encodes fibrinogen A alpha amino acids 1-625 with an initiating ATG in front of amino acid 1. The vector is an expression vector.
The depositor notes that the fibrinogen clones (ATCC 59706-59710) are suitable for applications in gene mapping or involving nucleic acid hybridization, but they are not suitable starting material for expression in mammalian cells.
The clones do not encode the signal peptide necessary for assembly and secretion and one is known to lack a single nucleotide in the coding region.
The ability of this probe to detect the TaqI polymorphism was verified by J. Murray, University of Iowa.
References:

Chung DW, et al. Characterization of complementary deoxyribonucleic acid and genomic deoxyribonucleic acid for the beta-chain of human fibronogen. Biochemistry 22: 3244-3250, 1983. PubMed: 6688356

Lord ST. Expression of a cloned human fibrinogen cDNA in Escherichia coli: synthesis of an A alpha polypeptide. DNA 4: 33-38, 1985. PubMed: 3882374

Susan T Lord, personal communication