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Fibrillin 2 Antikörper (AA 2740-2912)

Der Kaninchen Polyklonal Anti-Fibrillin 2-Antikörper wurde für ELISA und WB validiert. Er ist geeignet, Fibrillin 2 in Proben von Human zu detektieren.
Produktnummer ABIN7601047

Kurzübersicht für Fibrillin 2 Antikörper (AA 2740-2912) (ABIN7601047)

Target

Alle Fibrillin 2 (FBN2) Antikörper anzeigen
Fibrillin 2 (FBN2)

Reaktivität

  • 32
  • 7
  • 1
  • 1
  • 1
Human

Wirt

  • 33
  • 3
  • 2
Kaninchen

Klonalität

  • 35
  • 3
Polyklonal

Konjugat

  • 18
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Fibrillin 2 Antikörper ist unkonjugiert

Applikation

  • 16
  • 13
  • 13
  • 13
  • 9
  • 7
  • 7
  • 5
  • 3
  • 1
  • 1
ELISA, Western Blotting (WB)
  • Bindungsspezifität

    • 15
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    AA 2740-2912

    Verwendungszweck

    Anti-fibrillin 2/FBN2 Antibody Picoband®

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-fibrillin 2/FBN2 Antibody Picoband® (ABIN7601047). Tested in ELISA, WB applications. This antibody reacts with Human. 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 fibrillin 2/FBN2 recombinant protein (Position: N2740-Y2912).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Babcock, D., Gasner, C., Francke, U., Maslen, C. A single mutation that results in an asp-to-his substitution and partial exon skipping in a family with congenital contractual arachnodactyly. Hum. Genet. 103: 22-28, 1998. 2. Belleh, S., Zhou, G., Wang, M., Der Kaloustian, V. M., Pagon, R. A., Godfrey, M. Two novel fibrillin-2 mutations in congenital contractural arachnodactyly. Am. J. Med. Genet. 92: 7-12, 2000. 3. Lee, B., Godfrey, M., Vitale, E., Hori, H., Mattei, M.-G., Sarfarazi, M., Tsipouras, P., Ramirez, F., Hollister, D. W. Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes. Nature 352: 330-334, 1991.

    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

    Fibrillin 2 (FBN2)

    Andere Bezeichnung

    FBN2

    Hintergrund

    Synonyms: Vacuolar protein sorting-associated protein 4B, Cell migration-inducing gene 1 protein, Suppressor of K (+) transport growth defect 1, Protein SKD1, VPS4B, SKD1, VPS42, MIG1

    Tissue Specificity: Ubiquitously expressed.

    Background: Fibrillin is a glycoprotein, which is essential for the formation of elastic fibers found in connective tissue. The protein encoded by this gene is a component of connective tissue microfibrils and may be involved in elastic fiber assembly. Mutations in this gene cause congenital contractural arachnodactyly.

    Molekulargewicht

    315 kDa, 250 kDa

    Gen-ID

    2201

    UniProt

    P35556

    Pathways

    Maintenance of Protein Location, SARS-CoV-2 Protein Interaktom
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