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

DKC1 Antikörper (AA 81-190) (Cy7)

DKC1 Reaktivität: Human WB, IF (cc), IF (p) Wirt: Kaninchen Polyclonal Cy7
Produktnummer ABIN1708039
  • Target Alle DKC1 Antikörper anzeigen
    DKC1 (Dyskeratosis Congenita 1, Dyskerin (DKC1))
    Bindungsspezifität
    • 14
    • 10
    • 7
    • 6
    • 6
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 81-190
    Reaktivität
    • 73
    • 34
    • 26
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 71
    • 3
    • 1
    Kaninchen
    Klonalität
    • 64
    • 11
    Polyklonal
    Konjugat
    • 34
    • 6
    • 5
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Dieser DKC1 Antikörper ist konjugiert mit Cy7
    Applikation
    • 55
    • 27
    • 26
    • 25
    • 13
    • 13
    • 12
    • 10
    • 6
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Homologie
    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human Dyskerin
    Isotyp
    IgG
    Top Product
    Discover our top product DKC1 Primärantikörper
  • Applikationshinweise
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    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
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: 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
    DKC1 (Dyskeratosis Congenita 1, Dyskerin (DKC1))
    Andere Bezeichnung
    Dyskerin (DKC1 Produkte)
    Synonyme
    CBF5 antikoerper, DKC antikoerper, DKCX antikoerper, NAP57 antikoerper, NOLA4 antikoerper, XAP101 antikoerper, dyskerin antikoerper, fv62a07 antikoerper, wu:fa28f10 antikoerper, wu:fc87a02 antikoerper, wu:fi24a05 antikoerper, wu:fv62a07 antikoerper, zgc:110395 antikoerper, DKC1 antikoerper, cbf5 antikoerper, dkc antikoerper, nap57 antikoerper, nola4 antikoerper, xap101 antikoerper, BC068171 antikoerper, Nap57 antikoerper, AtCBF5 antikoerper, AtNAP57 antikoerper, homologue of NAP57 antikoerper, dyskerin pseudouridine synthase 1 antikoerper, microRNA 664b antikoerper, dyskeratosis congenita 1, dyskerin antikoerper, dyskeratosis congenita 1, dyskerin L homeolog antikoerper, homologue of NAP57 antikoerper, DKC1 antikoerper, MIR664B antikoerper, dkc1 antikoerper, dkc1.L antikoerper, Dkc1 antikoerper, NAP57 antikoerper
    Hintergrund

    Synonyms: CBF5, CBF5 homolog, Cbf5p homolog, DKC 1, DKC, Dkc1, DKC1_HUMAN, DKCX, Dyskeratosis congenita 1, Dyskeratosis congenita 1 dyskerin, Dyskerin, H/ACA ribonucleoprotein complex subunit 4, NAP 57, NAP57, NAP-57, NOLA 4, NOLA4, Nopp140 associated protein of 57 kDa, Nopp140-associated protein of 57 kDa, Nucleolar protein family A member 4, Nucleolar protein NAP57, snoRNP protein DKC1, XAP 101, XAP101.

    Background: Dyskerin (NAP57) associates with the chaperone protein Nopp140 and forms a small ribonucleoprotein particle with GAR1 (NOLA1), NHP2 (NOLA2) and Nop10 for the isomerization of uridine to pseudouridine (1). GAR1, NHP2 and dyskerin localize to the dense fibrillar component of the nucleolus and in nuclear Cajal bodies (2). The dyskerin gene maps to chromosome Xq28 (3). Missense mutations in the dyskerin gene interfere with normal nuclear localization of dyskerin and cause Dyskeratosis congenita (DKC) (4). DKC is a rare, X-linked bone marrow disorder characterized by cutaneous hyperpigmentation, dystrophy of the nails, atrophy of the testicles and leukoplakia of the oral mucosa. The GAR1 gene maps to chromosome 4q25 (5,6). The NHP2 gene maps to chromosome 5q35.3 and encodes a 155-amino acid protein (2,7).

    Gen-ID
    1736
    Pathways
    Telomere Maintenance
Sie sind hier:
Kundenservice