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SUMF2 Antikörper (AA 26-301)

Der Kaninchen Polyklonal Anti-SUMF2-Antikörper wurde für ELISA, WB, IHC, IF und FACS validiert. Er ist geeignet, SUMF2 in Proben von Human zu detektieren.
Produktnummer ABIN7600954

Kurzübersicht für SUMF2 Antikörper (AA 26-301) (ABIN7600954)

Target

Alle SUMF2 Antikörper anzeigen
SUMF2 (Sulfatase Modifying Factor 2 (SUMF2))

Reaktivität

  • 12
  • 3
  • 1
Human

Wirt

  • 8
  • 4
  • 1
Kaninchen

Klonalität

  • 9
  • 4
Polyklonal

Konjugat

  • 10
  • 1
  • 1
  • 1
Dieser SUMF2 Antikörper ist unkonjugiert

Applikation

  • 11
  • 10
  • 3
  • 3
  • 1
  • 1
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)
  • Bindungsspezifität

    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 26-301

    Verwendungszweck

    Anti-SUMF2 Antibody Picoband®

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-SUMF2 Antibody Picoband® (ABIN7600954). Tested in ELISA, Flow Cytometry, IF, IHC, 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 SUMF2 recombinant protein (Position: Q26-L301).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Human
    Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human
    Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Cosma, M. P., Pepe, S., Annunziata, I., Newbold, R. F., Grompe, M., Parenti, G., Ballabio, A. The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases. Cell 113: 445-456, 2003. 2. Dierks, T., Schmidt, B., Borissenko, L. V., Peng, J., Preusser, A., Mariappan, M., von Figura, K. Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C-alpha-formylglycine generating enzyme. Cell 113: 435-444, 2003. 3. Gross, M. B. Personal Communication. Baltimore, Md. 2/26/2015.

    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

    SUMF2 (Sulfatase Modifying Factor 2 (SUMF2))

    Andere Bezeichnung

    SUMF2

    Hintergrund

    Synonyms: Pannexin-2, PANX2

    Tissue Specificity: Expressed in fetal and adult brain. Also detected in fetal liver and skeletal muscle, but not in their adult counterparts.

    Background: Sulfatase-modifying factor 2 is an enzyme that in humans is encoded by the SUMF2 gene. The catalytic sites of sulfatases are only active if they contain a unique amino acid, C-alpha-formylglycine (FGly). The FGly residue is posttranslationally generated from a cysteine by enzymes with FGly-generating activity. The gene described in this record is a member of the sulfatase-modifying factor family and encodes a protein with a DUF323 domain that localizes to the lumen of the endoplasmic reticulum. This protein has low levels of FGly-generating activity but can heterodimerize with another family member - a protein with high levels of FGly-generating activity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

    Molekulargewicht

    36 kDa

    Gen-ID

    25870
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