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NBR1 Monoclonal Antibody

规格: / 20μL / 60μL / 120μL
价格: / ¥580 / ¥1420 / ¥2310

货号:E-AB-22148

宿主: Mouse

反应性: H,M,R

应用: IHC-p,IF

  • 详情
  • Overview

    Synonyms 1A1 3B,1A13B,B box protein,Cell migration-inducing gene 19 protein,KIAA0049,M17S2,Membrane component chromosome 17 surface marker 2,Membrane component,chromosome 17,surface marker 2 (ovarian carcinoma antigen CA125),MIG 19,MIG19,Migration inducing protein 19,NBR 1,Nbr1,NBR1,autophagy cargo receptor,NBR1,Neighbor of BRCA1 gene 1,Neighbor of BRCA1 gene 1 protein,Next to BRCA1 gene 1 protein,Ovarian carcinoma antigen CA125,Protein 1A1-3B,NBR1 Mouse (7C3)抗体
    Swissprot Q14596
    Source Mouse
    Reactivity Human,Mouse,Rat
    Immunogen Recombinant Protein of NBR1
    Application IHC-p(Detection kit: E-IR-R213),IF
    Recommended dilution IHC,,1:50-300;IF,,1:50-1:200;
    Concentration 1mg/mL
    Clonality Monoclonal

    Properties

    Cellular localization Cytoplasm. Cytoplasmic vesicle>autophagosome. Lysosome. Cytoplasm>myofibril>sarcomere>M line. In cardiac muscles localizes to the sarcomeric M line (By similarity). Is targeted to lysosomes for degradation.
    Clone No Clone:4C6
    Isotype IgG
    Purification Protein A purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.02% sodium azide, 50% glycerol, pH7.4
    Background The protein encoded by this gene was originally identified as an ovarian tumor antigen monitored in ovarian cancer. The encoded protein contains a B-box/coiled-coil motif, which is present in many genes with transformation potential. It functions as a specific autophagy receptor for the selective autophagic degradation of peroxisomes by forming intracellular inclusions with ubiquitylated autophagic substrates. This gene is located on a region of chromosome 17q21.1 that is in close proximity to the BRCA1 tumor suppressor gene. Alternative splicing of this gene results in multiple transcript variants.NBR1 (NBR1, Autophagy Cargo Receptor) is a Protein Coding gene. Diseases associated with NBR1 include Inclusion Body Myositis and Synucleinopathy. Among its related pathways are Mitophagy - animal. GO annotations related to this gene include ubiquitin binding and mitogen-activated protein kinase binding.
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