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Alexa Fluor® 647 Rat Anti-Mouse CD169 Antibody (S-R594)

Sialoadhesin,Sheep erythrocyte receptor (SER),Sialic acid-binding Ig-like lectin 1 (Siglec-1),Sa,Sn,Siglec1

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B80381
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD169
  • 分子别名

    Sialoadhesin; Sheep erythrocyte receptor (SER); Sialic acid-binding Ig-like lectin 1 (Siglec-1); Sa; Sn; Siglec1
  • 细胞定位

    Secreted, Cell membrane
  • Accession

    Q62230
  • 克隆号

    S-R594
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2a,k
  • 同型对照

    S0B8044
  • 反应种属 ?

    Ms
  • 阳性样本

    Fresh C57BL/6 mouse bone marrow
  • 纯化方式

    Protein G
  • 浓度

    0.5 mg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.3% Proclin 300

  • 储存条件

    12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

  • 应用

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 1μg per million cells in 100μl volume Ms
背景介绍
  • CD169, also known as Siglec-1 or sialoadhesin, is a type I transmembrane glycoprotein of the immunoglobulin superfamily expressed predominantly on subsets of tissue-resident macrophages and some dendritic cells; it contains 17 extracellular Ig-like domains that together project ~33 nm from the plasma membrane to enable high-avidity binding to α2,3-linked sialic acid moieties on glycoproteins and glycolipids of host cells or pathogens, thereby facilitating pathogen capture, antigen presentation, and adaptive immune priming while simultaneously serving as an entry portal for viruses such as HIV-1, PRRSV, and SARS-CoV-2, and its interferon-inducible expression correlates with both protective immunity and disease severity in infections, cancer, and chronic inflammatory disorders.

  • 流式分析

    • Flow cytometric analysis of CD169 expression on fresh C57BL/6 mouse bone marrow. Fresh C57BL/6 mouse bone marrow were stained with Pacific Blue™ Rat Anti-Mouse Ly6G/Ly6C Antibody and either Alexa Fluor® 647 Rat IgG2a, κ Isotype Control (left panel) or SDT Alexa Fluor® 647 Rat Anti- Mouse CD169 Antibody (right panel) at 2 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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