anti-CD8b antibody [341]

Key features and details

  • 产品描述: Mouse Monoclonal antibody [341] recognizes CD8b
  • 反应物种: Rat
  • 应用: FACS, FuncSt, IHC-Fr, IP, WB
  • 特异性: The clone 341 (also known as 34.1) recognizes rat CD8b, the 32-34 kDa beta chain of the CD8 coreceptor, expressed on T cell subsets and some other cell types, such as macrophages.
  • 宿主: Mouse
  • 克隆: Monoclonal
  • 克隆号: 341
  • 同位型: IgG1
  • 靶点名称: CD8b
  • Brand:
CAT.NO. : ARG65386
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Product Details
概述
产品描述Mouse Monoclonal antibody [341] recognizes CD8b
反应物种Rat
应用FACS, FuncSt, IHC-Fr, IP, WB
特异性The clone 341 (also known as 34.1) recognizes rat CD8b, the 32-34 kDa beta chain of the CD8 coreceptor, expressed on T cell subsets and some other cell types, such as macrophages.
宿主Mouse
克隆Monoclonal
克隆号341
同位型IgG1
靶点名称CD8b
抗原CD8 positive Wistar rat splenic T cell hybridomas
偶联标记Un-conjugated
別名LY3; CD8B1; CD antigen CD8b; LEU2; T-cell surface glycoprotein CD8 beta chain; P37; LYT3
应用说明
应用建议
应用推荐稀释比
FACS1.5 µg/ml
FuncStAssay-dependent
IHC-FrAssay-dependent
IPAssay-dependent
WBAssay-dependent
应用说明Functional studies: Macrophage stimulation, in vitro blocking of allogenic responses.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
属性
形式Liquid
纯化Purified from cell culture supernatant by protein-A affinity chromatography.
纯度> 95% (by SDS-PAGE)
缓冲液PBS (pH 7.4) and 15 mM Sodium azide
抗菌剂15 mM Sodium azide
浓度1 mg/ml
存放说明For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项For laboratory research only, not for drug, diagnostic or other use.
生物信息
数据库连接

GeneID: 24931 Rat CD8B

Swiss-port # P05541 Rat T-cell surface glycoprotein CD8 beta chain

基因名称Cd8b
全名CD8b molecule
背景介绍The CD8b (CD8 beta) subunit of CD8 T cell coreceptor is expressed in CD8 alpha/beta heterodimers on majority of MHC I-restricted conventional T cells and thymocytes and in CD8 alpha/alpha homodimers on subsets of memory T cells, intraepithelial lymphocytes, NK cells, macrophages, mast cells, and dendritic cells. Regulation of CD8 beta level on T cell surface seems to be an important mechanism to control their effector function. Assembly of CD8 alpha/beta but not alpha/alpha dimers is connected with formation or localization to the lipid rafts. Recruiting triggered TCR complexes to these membrane microdomains as well as affinity of TCR to MHC I is modulated by CD8, thereby affecting the functional diversity of the TCR signaling.
生物功能Identifies cytotoxic/suppressor T-cells that interact with MHC class I bearing targets. CD8 is thought to play a role in the process of T-cell mediated killing. [UniProt]
产品亮点Related products:
CD8 antibodies; CD8 ELISA Kits; CD8 Duos / Panels; Anti-Mouse IgG secondary antibodies;
Related news:
New antibody panels and duos for Tumor immune microenvironment
Tumor-Infiltrating Lymphocytes (TILs)
研究领域Immune System antibody
预测分子量24 kDa
翻译后修饰Phosphorylated as a consequence of T-cell activation.
检测图片 (2)
  • ARG65386 anti-CD8b antibody [341] FACS image

    Flow Cytometry: Rat splenocytes suspension stained with ARG65386 anti-CD8b antibody [341] at 1 µg/ml dilution, followed by PE-conjugated Goat anti-Mouse antibody.

  • ARG65386 anti-CD8b antibody [341] FACS image

    Flow Cytometry: Separation of Rat CD8b positive splenocytes (red-filled) from CD8b negative splenocytes (black-dashed). Rat splenocyte suspension stained with ARG65386 anti-CD8b antibody [341] at 1 µg/ml dilution, followed by PE-conjugated Goat anti-Mouse antibody.

参考文献

克隆号文献

Rapid recovery from T lymphopenia by CD28 superagonist therapy.

Elflein K et al.
Blood.,  (2003)

publication_link

 

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Mechanisms of macrophage stimulation through CD8: macrophage CD8alpha and CD8beta induce nitric oxide production and associated killing of the parasite Leishmania major.

Hirji N et al.
J Immunol.,  (1998)

publication_link

 

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