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protein genbank id gi number organism orf1594 yp 400611 1 81300403 synechococcus elongatus pcc7942 pmt9312  (ATCC)


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    ATCC protein genbank id gi number organism orf1594 yp 400611 1 81300403 synechococcus elongatus pcc7942 pmt9312
    Protein Genbank Id Gi Number Organism Orf1594 Yp 400611 1 81300403 Synechococcus Elongatus Pcc7942 Pmt9312, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/genbank+c/Saccharomyces+cerevisiae+Meyen+ex+E%2EC%2E+Hansen/us12398396-3831-0-32
    Average 94 stars, based on 1 article reviews
    protein genbank id gi number organism orf1594 yp 400611 1 81300403 synechococcus elongatus pcc7942 pmt9312 - by Bioz Stars, 2026-10
    94/100 stars

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    Article Title: Identification of an Important Orphan Histidine Kinase for the Initiation of Sporulation and Enterotoxin Production by Clostridium perfringens Type F Strain SM101
    Article Snippet: With two exceptions, these putative orphan kinase genes are also present in 7 other surveyed GenBank C. perfringens genomes (strain 13, F4969, ATCC 13124, ATCC 3626, JGS1495, JGS1721, and JGS1987), representing all C. perfringens types except type G. The two exceptions both involve type C strain JGS1495, which does not carry the cpr1055 gene or the cpr1316 gene.

    Article Title: Identification of an Important Orphan Histidine Kinase for the Initiation of Sporulation and Enterotoxin Production by Clostridium perfringens Type F Strain SM101
    Article Snippet: With two exceptions, these putative orphan kinase genes are also present in 7 other surveyed GenBank C. perfringens genomes (strain 13, F4969, ATCC 13124, ATCC 3626, JGS1495, JGS1721, and JGS1987), representing all C. perfringens types except type G. The two exceptions both involve type C strain JGS1495, which does not carry the cpr1055 gene or the cpr1316 gene.



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    Image Search Results


    a VHH60 inhibits pseudovirus carrying wildtype spike protein infection on Caco-2 cell line. b VHH60 inhibits ancestral SARS-CoV-2 infection on Vero-E6. c Survival curve of mice infected by SARS-CoV-2. Vehicle group all died at 4 d.p.i (5/5), one in VHH60 group (1/5) died. d Body weight change of mice infected by SARS-CoV-2. Data is represented as ratio of body weights at indicated timepoint versus day 0 ( n = 10 at 0 and 3 d.p.i, n = 4 at 4 d.p.i, n = 5 at 5.d.p.i). e Virus load in lung after 3 days of infection ( n = 5). f Representative image of immunofluorescence from lung. Blue: Nuclei, Red: ACE2, Green: nucleocapsid protein (NP). g Representative image of hematoxylin-eosin (H&E) staining from the lung. Scar bar, 2000 μm in the up row, 150 μm in the down row. One-way ANOVA with Tukey’s multiple comparison test was used. * P < 0.05. Error bars represent the means with SDs.

    Journal: Cell Death & Disease

    Article Title: A broad neutralizing nanobody against SARS-CoV-2 engineered from an approved drug

    doi: 10.1038/s41419-024-06802-7

    Figure Lengend Snippet: a VHH60 inhibits pseudovirus carrying wildtype spike protein infection on Caco-2 cell line. b VHH60 inhibits ancestral SARS-CoV-2 infection on Vero-E6. c Survival curve of mice infected by SARS-CoV-2. Vehicle group all died at 4 d.p.i (5/5), one in VHH60 group (1/5) died. d Body weight change of mice infected by SARS-CoV-2. Data is represented as ratio of body weights at indicated timepoint versus day 0 ( n = 10 at 0 and 3 d.p.i, n = 4 at 4 d.p.i, n = 5 at 5.d.p.i). e Virus load in lung after 3 days of infection ( n = 5). f Representative image of immunofluorescence from lung. Blue: Nuclei, Red: ACE2, Green: nucleocapsid protein (NP). g Representative image of hematoxylin-eosin (H&E) staining from the lung. Scar bar, 2000 μm in the up row, 150 μm in the down row. One-way ANOVA with Tukey’s multiple comparison test was used. * P < 0.05. Error bars represent the means with SDs.

    Article Snippet: The constructs of VHHs were selected from phage display, RBD fragment (aa319-541) of SARS-CoV-2 S protein (GenBank: MN908947.3) was synthesized by Genewiz Inc, the extracellular domain of human ACE2 (1-740 aa) (GenBank: NM_021804.1) was amplified from a plasmid (Cat. # HG10108-ACG, Sinobiologic).

    Techniques: Infection, Virus, Immunofluorescence, Staining, Comparison

    a Cryo-EM for the Spike-VHH60 complex observed to a resolution of 3.79 Å, revealing binding of VHH60 to RBDs in the “1-up” conformation. b Comparison of the epitope between VHH60 (light sea green) and VHH72 (salmon, PDB ID: 6WAQ). c CDR loops of VHH60 (cornflower) overlaid on the surface epitope (salmon) representation of RBD (light sea green). d The hydrogen bonds at the binding interface between VHH60 and SARS-CoV-2 RBD based on the crystal structure of the complex at 3.40 Å. e Superposition of the RBD-ACE2 model (PDB ID:7XO9) to that of the VHH60- RBD model shows there is a steric hindrance between VHH60 and ACE2.

    Journal: Cell Death & Disease

    Article Title: A broad neutralizing nanobody against SARS-CoV-2 engineered from an approved drug

    doi: 10.1038/s41419-024-06802-7

    Figure Lengend Snippet: a Cryo-EM for the Spike-VHH60 complex observed to a resolution of 3.79 Å, revealing binding of VHH60 to RBDs in the “1-up” conformation. b Comparison of the epitope between VHH60 (light sea green) and VHH72 (salmon, PDB ID: 6WAQ). c CDR loops of VHH60 (cornflower) overlaid on the surface epitope (salmon) representation of RBD (light sea green). d The hydrogen bonds at the binding interface between VHH60 and SARS-CoV-2 RBD based on the crystal structure of the complex at 3.40 Å. e Superposition of the RBD-ACE2 model (PDB ID:7XO9) to that of the VHH60- RBD model shows there is a steric hindrance between VHH60 and ACE2.

    Article Snippet: The constructs of VHHs were selected from phage display, RBD fragment (aa319-541) of SARS-CoV-2 S protein (GenBank: MN908947.3) was synthesized by Genewiz Inc, the extracellular domain of human ACE2 (1-740 aa) (GenBank: NM_021804.1) was amplified from a plasmid (Cat. # HG10108-ACG, Sinobiologic).

    Techniques: Cryo-EM Sample Prep, Binding Assay, Comparison