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LRRC75A/FAM211A 抗体 (AA 52-292)

The 兔 多克隆 anti-LRRC75A/FAM211A antibody is suitable to detect LRRC75A/FAM211A in samples from 人. It has been validated for WB, ELISA 和 FACS.
产品编号 ABIN7875558
发货至: 中国
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Quick Overview for LRRC75A/FAM211A 抗体 (AA 52-292) (ABIN7875558)

抗原

LRRC75A/FAM211A (LRRC75A) (Leucine Rich Repeat Containing 75A (LRRC75A))

适用

宿主

  • 2

克隆类型

  • 2
多克隆

标记

  • 2
This LRRC75A/FAM211A antibody is un-conjugated

应用范围

Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • 抗原表位

    • 1
    • 1
    AA 52-292

    原理

    LRRC75A Antibody / FAM211A

    纯化方法

    Antigen affinity purified

    免疫原

    An E.coli-derived human recombinant protein (amino acids H52-Q292) was used as the immunogen for the LRRC75A antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the LRRC75A antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the LRRC75A antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    LRRC75A/FAM211A (LRRC75A) (Leucine Rich Repeat Containing 75A (LRRC75A))

    别名

    LRRC75A

    背景

    Long noncoding RNAs (lncRNAs) play multiple key roles during inflammatory processes. A novel lncRNA identified by the high-throughput sequencing analysis was found significantly down-regulated in Escherichia coli-introduced cell model of bovine mastitis. Given that this lncRNA consists of the antisense of leucine-rich repeat-containing protein 75A (LRRC75A), it was named LRRC75A antisense lncRNA1 (LRRC75A-AS1). The expression of LRRC75A-AS1 was down-regulated in bovine mammary epithelial cells and mammary tissues under inflammatory condition. Knockout (KO) of LRRC75A-AS1 by CRISPR-Cas9 system in bovine mammary alveolar cell-T (MAC-T) cell line could enhance expressions of tight junction (TJ) proteins Claudin-1, Occludin and ZO-1, reduce cell monolayer permeability, and inhibit Staphylococcus aureus adhesion and invasion. Meanwhile, it also down-regulated expressions of inflammatory factors and attenuated activation of NF-?B pathway. Similarly, knockdown of LRRC75A caused the changes as LRRC75A-AS1 KO did, while overexpression of LRRC75A enabled the opposite effects. TJ of epithelioid cells barriers the pathogenic microorganisms outside during inflammation, in which LRRC75A-AS1 can regulate the expression of TJ proteins through LRRC75A, affecting the development of inflammation.

    UniProt

    Q8NAA5
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