Maltose phosphorylase antibody (Peroxidase)

Katalog-Nummer orb344261-100ug

Size : 100ug

Marke : Biorbyt

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    Maltose phosphorylase antibody (Peroxidase)

    Catalog Number: orb344261

    Catalog Numberorb344261
    CategoryAntibodies
    DescriptionMaltose phosphorylase antibody (Peroxidase)
    Species/HostGoat
    ClonalityPolyclonal
    Tested applicationsELISA, IP, WB
    ReactivityBacteria
    IsotypeIgG
    ImmunogenMaltose Phosphorylase [E.coli]
    Concentration1 mg/mL
    Dilution rangeELISA: 1:5,000 - 1:20,000, IP: 1:100, WB: 1:500 - 1:5,000
    Form/AppearanceLyophilized
    PurityMaltose Phosphorylase is an IgG fraction antibody purified from monospecific antiserum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Peroxidase, anti-Goat Serum as well as purified and partially purified Maltose Phosphorylase [E.coli]. Cross reactivity against Maltose Phosphorylase from other sources is unknown.
    ConjugationHRP
    UniProt IDB2GEX2
    NCBIYP_001842841.1
    StorageStore vial at 4° C prior to restoration. For extended storage aliquot contents and freeze at -20° C or below. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.
    Buffer/Preservatives0.01% (w/v) Gentamicin Sulfate. Do NOT add Sodium Azide!
    Alternative namesgoat anti-Maltose Phosphorylase Antibody HRP Conju
    NoteFor research use only
    Application notesAnti-Maltose Phosphorylase has a working dilution of 1:2,000 to 1:10,000 of the reconstitution concentration is suggested for this product.
    Expiration Date12 months from date of receipt.
    Maltose phosphorylase antibody (Peroxidase)

    Biorbyt Goat anti Maltose Phosphorylase antibody was used to detect Maltose Phosphorylase under reducing (R) and non-reducing (NR) conditions. Reduced samples of purified target proteins contained 4% BME and were boiled for 5 minutes. Samples of ~1 ug of protein per lane were run by SDS-PAGE. Protein was transferred to nitrocellulose and probed with 1:3000 dilution of primary antibody (ON 4 C in orb348637). Detection shown was using Dylight 488 conjugated Donkey anti goat (1:10K in TBS/orb348637 1 hr RT).