SAB5300165
单克隆抗 OVA 小鼠抗
clone 3G2E1D9, ascites fluid
别名:
N/A
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关于此项目
NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
3G2E1D9, monoclonal
Application:
ELISA (d), WB
Citations:
4
biological source
mouse
conjugate
unconjugated
antibody form
ascites fluid
antibody product type
primary antibodies
clone
3G2E1D9, monoclonal
technique(s)
direct ELISA: 1:10,000, western blot: 1:500-1:2,000
isotype
IgG1
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
General description
卵清蛋白（323-339）是由B细胞表位环绕的蛋清蛋白，被特异性IgE抗体结合。除此之外，它还含有CD4+ T细胞表位。
Immunogen
卵清蛋白
小鼠抗卵清蛋白单克隆抗体
小鼠抗卵清蛋白单克隆抗体
Biochem/physiol Actions
卵清蛋白（OVA）肽323-339在隔离的BALB/c小鼠体内介导25-35%的T细胞对完整OVA的反应。OVA 323-339被广泛用于测定第II类主要组织相容性复合体（MHC）-肽结合特征和T细胞活化特征。它被广泛用于过敏研究。
Physical form
含 0.03% 叠氮化钠的腹水。
Disclaimer
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存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
常规特殊物品
动植物来源生物产品
此项目有
Keigo Kondou et al.
Journal of biological engineering, 13, 77-77 (2019-10-28)
The baculovirus (BV) Autographa californica multiple nuclear polyhedrosis virus has been used in numerous protein expression systems because of its ability to infect insect cells and serves as a useful vaccination vector with several benefits, such as its low clinical
Comparison between ovalbumin and ovalbumin peptide 323-339 responses in allergic mice: humoral and cellular aspects.
Sun LZ
Scandinavian Journal of Immunology, 71(5), 329-335 (2010)
Ingrid S Zeelenberg et al.
Cancer research, 68(4), 1228-1235 (2008-02-19)
Expression of non-self antigens by tumors can induce activation of T cells in vivo, although this activation can lead to either immunity or tolerance. CD8+ T-cell activation can be direct (if the tumor expresses MHC class I molecules) or indirect
Tian-Yu Song et al.
Nature communications, 12(1), 7003-7003 (2021-12-03)
Cancer cells acquire genetic heterogeneity to escape from immune surveillance during tumor evolution, but a systematic approach to distinguish driver from passenger mutations is lacking. Here we investigate the impact of different immune pressure on tumor clonal dynamics and immune
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