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Results for "

p 67

" in TargetMol Product Catalog
  • Inhibitor Products
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  • Recombinant Protein
    6
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p67phox Protein, Human, Recombinant (His & GST)
TMPY-03619
p67phox Protein, Human, Recombinant (His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 87.6 kDa and the accession number is AAH01606.1.
  • $600
7-10 days
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SARS-CoV-2 Nucleocapsid Protein (P67S, His)
TMPY-06221
SARS-CoV-2 Nucleocapsid Protein (P67S, His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 46.6 kDa and the accession number is P0DTC9.
  • $698
7-10 days
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SARS-CoV-2 Nucleocapsid Protein (P67S & R203M & D377Y, His)
TMPY-06222
SARS-CoV-2 Nucleocapsid Protein (P67S & R203M & D377Y, His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 46.6 kDa and the accession number is P0DTC9.
  • $698
7-10 days
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p67phox Protein, Human, Recombinant
TMPY-03660
p67phox Protein, Human, Recombinant is expressed in Baculovirus insect cells. The predicted molecular weight is 30 kDa and the accession number is AAH01606.1.
  • $600
7-10 days
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SARS-CoV-2 Nucleocapsid Protein (P67S & P199L, His)
TMPY-06219
SARS-CoV-2 Nucleocapsid Protein (P67S & P199L, His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 46.6 kDa and the accession number is P0DTC9.
  • $698
7-10 days
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Munc18-1/STXBP1 Protein, Human, Recombinant (His & GST)
TMPY-01820
Syntaxin-binding protein 1, also known as N-Sec1, Protein unc-18 homolog 1, MUNC18-1 and STXBP1, is a peripheral membrane protein that belongs to the STXBP / unc-18 / SEC1 family. STXBP1 is an evolutionally conserved neuronal Sec1/Munc-18 (SM) protein that is essential in synaptic vesicle release in several species. It may participate in the regulation of synaptic vesicle docking and fusion, possibly through interaction with GTP-binding proteins. STXBP1 is essential for neurotransmission and binds syntaxin, a component of the synaptic vesicle fusion machinery probably in a 1:1 ratio. It can interact with syntaxins 1, 2, and 3 but not syntaxin 4. STXBP1 may also play a role in determining the specificity of intracellular fusion reactions. Defects in STXBP1 are the cause of epileptic encephalopathy early infantile type 4 (EIEE4). Affected individuals have neonatal or infantile onset of seizures, suppression-burst pattern on EEG, profound mental retardation, and MRI evidence of hypomyelination.
  • $700
7-10 days
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