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Lamin B2 Antikörper (AA 128-585)

Der Kaninchen Polyklonal Anti-Lamin B2-Antikörper wurde für WB, IHC und ELISA validiert. Er ist geeignet, Lamin B2 in Proben von Human und Ratte zu detektieren.
Produktnummer ABIN7599906

Kurzübersicht für Lamin B2 Antikörper (AA 128-585) (ABIN7599906)

Target

Alle Lamin B2 (LMNB2) Antikörper anzeigen
Lamin B2 (LMNB2)

Reaktivität

  • 61
  • 42
  • 20
  • 10
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Ratte

Wirt

  • 58
  • 19
Kaninchen

Klonalität

  • 54
  • 23
Polyklonal

Konjugat

  • 46
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Lamin B2 Antikörper ist unkonjugiert

Applikation

  • 58
  • 20
  • 17
  • 15
  • 13
  • 13
  • 11
  • 10
  • 9
  • 8
  • 8
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Bindungsspezifität

    • 15
    • 8
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 128-585

    Verwendungszweck

    Anti-Lamin B2/LMNB2 Antibody Picoband®

    Produktmerkmale

    Anti-Lamin B2/LMNB2 Antibody Picoband® (ABIN7599906). Tested in WB, IHC, Flow Cytometry, ELISA applications. This antibody reacts with Human, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human Lamin B2/LMNB2 recombinant protein (Position: L128-E585). Human LMNB2 shares 81.8% amino acid (aa) sequence identity with mouse LMNB2.
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Human
    Immunohistochemistry, 2-5 μg/mL, Human, Rat
    ELISA, 0.1-0.5 μg/mL, -
    1. Biamonti, G., Giacca, M., Perini, G., Contreas, G., Zentilin, L., Weighardt, F., Guerra, M., Della Valle, G., Saccone, S., Riva, S., Falaschi, A. The gene for a novel human lamin maps at a highly transcribed locus of chromosome 19 which replicates at the onset of S-phase. Molec. Cell. Biol. 12: 3499-3506, 1992. 2. Damiano, J. A., Afawi, Z., Bahlo, M., Mauermann, M., Misk, A., Arsov, T., Oliver, K. L., Dahl, H.-H. M., Shearer, A. E., Smith, R. J. H., Hall, N. E., Mahmood, K., Leventer, R. J., Scheffer, I. E., Muona, M., Lehesjoki, A.-E., Korczyn, A. D., Herrmann, H., Berkovic, S. F., Hildebrand, M. S. Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia. Hum. Molec. Genet. 24: 4483-4490, 2015. 3. Gao, J., Li, Y., Fu, X., Luo, X. A Chinese patient with acquired partial lipodystrophy caused by a novel mutation with LMNB2 gene. J. Pediat. Endocr. Metab. 25: 375-377, 2012.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Konzentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

    Lamin B2 (LMNB2)

    Andere Bezeichnung

    Lamin B2/LMNB2

    Hintergrund

    Lamin B2 is a protein that in humans is encoded by the LMNB2 gene. This gene encodes a B type nuclear lamin. The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Mutations in this gene are associated with acquired partial lipodystrophy.

    Molekulargewicht

    72 kDa

    Gen-ID

    84823

    UniProt

    Q03252

    Pathways

    Apoptose, Caspase Kaskade in der Apoptose
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