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MTTK-MERRF
MTTK-MERRF
规格:
货期:
编号:TS189802
品牌:Testobio
产品名称: MTTK-MERRF
商品货号: TS189802
Designations: MTTK-MERRF
GenBank Number:

J01415

Species: Homo sapiens, human
Depositors: DC Wallace
Applications:
EcoRI with FspI or SpeI can also be used to excise the insert.
Vector:
Construct size (kb): 8.779999732971191
Insert:
DNA: cDNA
Insert lengths(kb): 1.529000043869019
Tissue: muscle
Gene product: tRNA, lysine, mitochondrial MTTD
Insert Size (kb): 1.529
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: freeze-dried bacteria-free phage
Comments:
Restriction digests of the clone give the following sizes (kb): PstI/HindIII--7.3, 1.55; EcoRI/PvuI--9.0; EcoRI--9.0; ClaI--6.0, 2.8; BglII--9.0.
Digestion with HincII gives fragments (bp) of 956, 472, 144, and 54; with Hinf1 of 797, 528, 170, 79, and 52; and with Hpa2 of 803, 747, and 38 from the insert.
EcoRI with FspI or SpeI can also be used to excise the insert. EcoRI and FspI cut within the vector and SpeI cuts at nt 8739 (in ATP6).
Contains human mitochondrial DNA from nucleotide 7392 to 8921. The insert contains the mutation (A to G) at nucleotide 8344 in the tRNA-Lys gene, creating a CviJI restriction site, which has been identified as the cause of MERRF.
Constructed from a PCR product made with linkers to create a PstI site at the nt 7392 end and a HindIII site at the nt 8921 end.
References:

Shoffner JM, et al. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. Cell 61: 931-937, 1990. PubMed: 2112427

Wallace DC, et al. Familial mitochondrial encephalomyopahty (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease. Cell 55: 601-610, 1988. PubMed: 3180221

Douglas C Wallace, personal communication

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MTTK-MERRF

  • 货号: TS189802
  • 好评
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  • 品牌 : TESTOBIO
产品名称: MTTK-MERRF
商品货号: TS189802
Designations: MTTK-MERRF
GenBank Number:

J01415

Species: Homo sapiens, human
Depositors: DC Wallace
Applications:
EcoRI with FspI or SpeI can also be used to excise the insert.
Vector:
Construct size (kb): 8.779999732971191
Insert:
DNA: cDNA
Insert lengths(kb): 1.529000043869019
Tissue: muscle
Gene product: tRNA, lysine, mitochondrial MTTD
Insert Size (kb): 1.529
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: freeze-dried bacteria-free phage
Comments:
Restriction digests of the clone give the following sizes (kb): PstI/HindIII--7.3, 1.55; EcoRI/PvuI--9.0; EcoRI--9.0; ClaI--6.0, 2.8; BglII--9.0.
Digestion with HincII gives fragments (bp) of 956, 472, 144, and 54; with Hinf1 of 797, 528, 170, 79, and 52; and with Hpa2 of 803, 747, and 38 from the insert.
EcoRI with FspI or SpeI can also be used to excise the insert. EcoRI and FspI cut within the vector and SpeI cuts at nt 8739 (in ATP6).
Contains human mitochondrial DNA from nucleotide 7392 to 8921. The insert contains the mutation (A to G) at nucleotide 8344 in the tRNA-Lys gene, creating a CviJI restriction site, which has been identified as the cause of MERRF.
Constructed from a PCR product made with linkers to create a PstI site at the nt 7392 end and a HindIII site at the nt 8921 end.
References:

Shoffner JM, et al. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. Cell 61: 931-937, 1990. PubMed: 2112427

Wallace DC, et al. Familial mitochondrial encephalomyopahty (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease. Cell 55: 601-610, 1988. PubMed: 3180221

Douglas C Wallace, personal communication

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