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NDUFAF7 Antikörper (AA 101-200) (Alexa Fluor 350)

NDUFAF7 Reaktivität: Human WB, IF (cc), IF (p) Wirt: Kaninchen Polyclonal Alexa Fluor 350
Produktnummer ABIN1694205
  • Target Alle NDUFAF7 Antikörper anzeigen
    NDUFAF7 (NADH Dehydrogenase (Ubiquinone) Complex I, Assembly Factor 7 (NDUFAF7))
    Bindungsspezifität
    • 14
    • 2
    • 1
    AA 101-200
    Reaktivität
    • 17
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 17
    Kaninchen
    Klonalität
    • 17
    Polyklonal
    Konjugat
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser NDUFAF7 Antikörper ist konjugiert mit Alexa Fluor 350
    Applikation
    • 17
    • 12
    • 12
    • 3
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Homologie
    Human,Mouse,Rat,Cow,Sheep,Pig,Rabbit
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C2orf56
    Isotyp
    IgG
    Top Product
    Discover our top product NDUFAF7 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
    NDUFAF7 (NADH Dehydrogenase (Ubiquinone) Complex I, Assembly Factor 7 (NDUFAF7))
    Andere Bezeichnung
    C2orf56 (NDUFAF7 Produkte)
    Synonyme
    C11H2orf56 antikoerper, 2410091C18Rik antikoerper, AL033374 antikoerper, PRO1853 antikoerper, C2orf56 antikoerper, MidA antikoerper, c2orf56 antikoerper, NADH:ubiquinone oxidoreductase complex assembly factor 7 antikoerper, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex assembly factor 7 antikoerper, NADH:ubiquinone oxidoreductase complex assembly factor 7 S homeolog antikoerper, NDUFAF7 antikoerper, Ndufaf7 antikoerper, ndufaf7.S antikoerper
    Hintergrund

    Synonyms: C2orf56, Chromosome 2 open reading frame 56, MidA, MIDA_HUMAN, mitochondrial, Mitochondrial dysfunction protein A homolog, OTTHUMP00000158583, OTTHUMP00000201359, OTTHUMP00000201362, PRO1853, Protein midA homolog, Protein midA homolog, mitochondrial.

    Background: C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

    Gen-ID
    55471
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