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Herpes Simplex Virus 2 / HSV2 ( Glycoprotein D) Protein

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SKU
BIN019
Herpes Simplex Virus 2 / HSV2 Glycoprotein D recombinant protein, 1 mg
Size:
1 mg
  $1,415.00
2 Weeks*
Bulk/Customize
Specifications
Specifications
Product Data
Expression Host Pichia pastoris
Concentration lot specific
Purity Verified by SDS PAGE (Followed by Coomassie staining).
Presentation State Azide Free
Buffer Presentation State: Azide Free
State: Liquid purified protein
Buffer System: 0.02M Sodium Phosphate, 0.2M Sodium Chloride, 0.1 mM EDTA, pH 7.0 +/- 0.2
Preparation Liquid purified protein
Recommended Dilution Suitable for ELISA and Western blot.
Protein Description Recombinant Herpes Simplex Virus-2 (HSV-2), Glycoprotein D (gD). Glycosylated recombinant ecto-domain of HSV-2 gD. Sugars added to the protein result in a protein of heterogeneous size, all of which react with Human positive sera and monoclonal antibodies in ELISA and Western blot.
Storage Store at -20° to -70°C.
Aliquot to avoid multiple freeze/thaw cycles.
Stability Shelf life: six months from despatch.
Shipping Blue Ice
Reference Data
Synonyms HHV2
Summary Description: Purified recombinant ecto-domain of HSV-2gD, which was expressed in Pichia pastoris.
Protein Families Suitable for ELISA and Western blot.
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Documents
Resources

file-alt Citations

Simplexviruses Successfully Adapt to Their Host by Fine-Tuning Immune Responses
Mozzi, Cagliani, Pontremoli et al
Mol Biol Evol (2022) 39 (7) DOI: 10.1093/molbev/msac142
Cited by 13
AI Summary: OriGene contributed to this study by synthesizing and cloning the coding sequences of ICP47 N-terminus from HSV-1, HSV-2, and B-virus, as well as their mutagenized versions, into the pCMV6-Entry vector (custom service), enabling functional analysis of immune response modulation by these viral proteins.
Snippet: Western-Blot The coding sequences of ICP47 N-terminus from HSV-1 (55aa, YP_009137148), HSV-2 (55aa, YP_009137225.1), and B-virus (56aa, NP_851932) were synthesized and cloned in pCMV6-Entry vector by Origene custom service. The pCMV6 vectors coding for the corresponding mutagenized sequences were synthesized and cloned as well (fig. 4B). Jurkat cells were cultured in Roswell Park Memorial Institu
FigureFigureFigure
WB
Herpes simplex virus ICP27 regulates alternative pre-mRNA polyadenylation and splicing in a sequence-dependent manner
Tang, Patel, Krause
PNAS (2016) 113 (43), 12256-12261 DOI: 10.1073/pnas.1609695113
AI Summary: OriGene contributed to this study by synthesizing the 90 bp HSV-2 ICP34.5 exon 1 sequences ("pICP34.5-K8"), which were used to construct plasmids for investigating ICP27-mediated splicing regulation.
Snippet: The exact mutations are labeled in Fig. 4E. pICP34.5(−90+29) was cloned by inserting the ICP34.5 sequence amplified by oST708 and oST430 into pFlag vector at the EcoRI site. pICP34.5-K8 was constructed by synthesizing (Origene) 90 bp HSV-2 ICP34.5 exon 1 sequences,
Showing 1-2 of 2 papers.
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