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    CXCR1 Antibody

    Catalog Number: orb1671592

    DispatchUsually dispatched within 5-10 working days
    $ 888.00
    Catalog Numberorb1671592
    CategoryAntibodies
    DescriptionCXCR1 Antibody
    ClonalityRecombinant
    Clone NumberSE2
    Tested applicationsFC, IHC, WB
    ReactivityHuman
    IsotypeIgG kappa
    ImmunogenThis antibody was raised by immunizing BALB/c mice with a BSA-conjugated peptide comprising of the N-terminal part of IL-8RA (amino acids 1-30).
    Concentrationbatch dependent
    ConjugationUnconjugated
    TargetCXCR1
    UniProt IDP25024
    StorageStore at 4°C for up to 3 months. For longer storage, aliquot and store at -20°C.
    Buffer/PreservativesPBS with 0.02% Proclin 300.
    Alternative namesCXCR-1, C-X-C chemokine receptor type 1, CXC-R1, C
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    CXCR1 Antibody

    Western Blot using anti-IL-8RA antibody SE2. Human lymph node tissue lysates (35 ug protein in RIPA buffer) were resolved on a SDS PAGE gel and blots were probed with the chimeric rsion of SE2 (orb1671592) at 0.1 ug/ml before detection using an anti-rondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.

    CXCR1 Antibody

    Immunofluorescence staining of fixed human peripheral blood leukocytes with anti-IL-8RA antibody SE2. Immunofluorescence analysis of paraformaldehyde fixed human peripheral blood leukocytes on Shi-fix™ coverslips stained with the chimeric r version of SE2 (orb1671592) at 10 ug/ml for 1h followed by Alexa Fluor® 488 secondary antibody (2 ug/ml)- showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right- top-bottom orb1671592- DAPI- merged channels and an isotype control. The isotype control was an unknown specificity antibody (.1) followed by staining with Alexa Fluor® 488 secondary antibody.

    CXCR1 Antibody

    Flow cytometry using the Anti-IL-8RA antibody SE2 (Paraformaldehyde fixed human peripheral blood monocytes were stained with anti-unknown specificity antibody (3.0; isotype control - black line) or the r version of SE2 (orb1671592 - blue line) at a dilution of 1:100 for 1h at RT. After washing- the bound antibody was detected using a goat anti-r AlexaFluor® 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.

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