Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

NCMAP Antikörper (PE)

NCMAP Reaktivität: Human, Maus, Ratte WB Wirt: Kaninchen Polyclonal PE
Produktnummer ABIN1712761
  • Target Alle NCMAP Produkte
    NCMAP (Noncompact Myelin Associated Protein (NCMAP))
    Reaktivität
    • 24
    • 4
    • 4
    • 4
    • 4
    • 4
    Human, Maus, Ratte
    Wirt
    • 24
    Kaninchen
    Klonalität
    • 24
    Polyklonal
    Konjugat
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser NCMAP Antikörper ist konjugiert mit PE
    Applikation
    • 19
    • 13
    • 13
    • 7
    • 3
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Homologie
    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C1orf130
    Isotyp
    IgG
  • Applikationshinweise
    FCM(1:20-100)
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Haltbarkeit
    12 months
  • Target
    NCMAP (Noncompact Myelin Associated Protein (NCMAP))
    Andere Bezeichnung
    C1orf130 (NCMAP Produkte)
    Synonyme
    C1orf130 antikoerper, MP11 antikoerper, A330049M08Rik antikoerper, AA545175 antikoerper, Mp11 antikoerper, non-compact myelin associated protein antikoerper, noncompact myelin associated protein antikoerper, NCMAP antikoerper, Ncmap antikoerper
    Hintergrund

    Synonyms: C1orf130, CA130_HUMAN, Uncharacterized protein C1orf130.

    Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf130 gene product has been provisionally designated C1orf130 pending further characterization.

    Gen-ID
    400746
Sie sind hier:
Kundenservice