Recombinant Escherichia coli O157:H7 Long-chain-fatty-acid--CoA ligase (fadD)
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Catalog number
MBS1298355
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Price
Please ask
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Size
0.1 mg (Baculovirus)
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Products_type
Recombinant Protein
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Products_short_name
[Long-chain-fatty-acid--CoA ligase (fadD)]
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Other_names
[long-chain-fatty-acid--CoA ligase; Long-chain-fatty-acid--CoA ligase; Long-chain acyl-CoA synthetase; Acyl-CoA synthetase]
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Products_gene_name
[fadD]
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Products_gene_name_syn
[fadD]
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Other_gene_names
[fadD; oldD; Acyl-CoA synthetase]
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Purity
>85% (SDS-PAGE)
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Form
Lyophilized or liquid (Format to be determined during the manufacturing process)
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Storage_stability
Store at -20 degrees C. For long-term storage, store at -20 degrees C or -80 degrees C. Store working aliquots at 4 degrees C for up to one week. Repeated freezing and thawing is not recommended.
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Source
Recombinants or rec. proteins
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Group
recombinants
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Gene target
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Short name
Recombinant Escherichia coli O157:H7 Long-chain-fatty-acid--CoA ligase (fadD)
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Technique
Recombinant, E. coli recombinant proteins are genetic recombinations in Escherichia coli, supplied as white sterile powder lyopillized. MyBioSource advises they will be reconstituted in a buffer soluion or culture medium for cell culture.
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Host
E Coli or Yeast or Baculovirus or Mammalian Cell, Escherichia coli
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Alternative name
Rec. Escherichia coli O157:H7 large-epitope-fatty-acid--CoA ligase (Fas (tumor necrosis factor receptor superfamily, member 6) (TNFRSF6)-associated via death domain)
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Alternative technique
rec, escherichia
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Alternative to gene target
Fas (TNFRSF6)-associated via death domain, MORT1, FADD and IDBG-62144 and ENSG00000168040 and 8772, identical protein binding, Plasma membranes, Fadd and IDBG-212910 and ENSMUSG00000031077 and 14082, FADD and IDBG-645056 and ENSBTAG00000018274 and 493720
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MeSH Data
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Name
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Concept
Scope note:
A DNA amplification technique based upon the ligation of OLIGONUCLEOTIDE PROBES. The probes are designed to exactly match two adjacent sequences of a specific target DNA. The chain reaction is repeated in three steps in the presence of excess probe: (1) heat denaturation of double-stranded DNA, (2) annealing of probes to target DNA, and (3) joining of the probes by thermostable DNA ligase. After the reaction is repeated for 20-30 cycles the production of ligated probe is measured.
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Tree numbers
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Qualifiers
ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
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