HIV (GP120) fragment (318-327)

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HIV (GP120) fragment (318-327) Basic information
Product Name:HIV (GP120) fragment (318-327)
Synonyms:ARG-GLY-PRO-GLY-ARG-ALA-PHE-VAL-THR-ILE;HIV (GP120) (318-327);H-ARG-GLY-PRO-GLY-ARG-ALA-PHE-VAL-THR-ILE-OH;LYS-ALA-ARG-VAL-NLE-PHE: NO2-GLU-ALA-NLE-NH2 [KARV-NLE-F: NO2-EA-NLE-NH2];I-10, P18IIIB I10;L-Isoleucine, L-arginylglycyl-L-prolylglycyl-L-arginyl-L-alanyl-L-phenylalanyl-L-valyl-L-threonyl-;HIV (GP120) fragment (318-327)
CAS:147841-68-7
MF:C48H80N16O12
MW:1073.25
EINECS:
Product Categories:
Mol File:Mol File
HIV (GP120) fragment (318-327) Structure
HIV (GP120) fragment (318-327) Chemical Properties
density 1.43±0.1 g/cm3(Predicted)
storage temp. -15°C
pka3.36±0.10(Predicted)
SequenceArg-Gly-Pro-Gly-Arg-Ala-Phe-Val-Thr-Ile
InChIKeyOPTVPTKXPSEPBD-JLHVISHLSA-N
Safety Information
MSDS Information
HIV (GP120) fragment (318-327) Usage And Synthesis
UsesHIV gp120 (318-327) is a short sequence of the HIV-1 strain IIIB envelope peptide (rgpgrafvti) that corresponds to the conserved C-terminal region of the glycoprotein. HIV gp120 (318-327) is part of the HIV vaccine V3 peptide epitope, also known as the I10 peptide. However, HIV gp120 (318-327) lacks the A2 anchor residues recognized by epitope-specific CTLs but has structural features that confer promiscuous A2 binding[1][2].
References[1] Kmieciak D, et al. The effect of deletion of the V3 loop of gp120 on cytotoxic T cell responses and HIV gp120-mediated pathogenesis. J Immunol. 1998 Jun 1;160(11):5676-83. PMID:9605175
[2] Gu L, et al. A recombinant adenovirus-based vector elicits a specific humoral immune response against the V3 loop of HIV-1 gp120 in mice through the "Antigen Capsid-Incorporation" strategy. Virol J. 2014 Jun 16;11:112. DOI:10.1186/1743-422X-11-112
HIV (GP120) fragment (318-327) Preparation Products And Raw materials
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