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Ectodysplasin A Antikörper (AA 30-391)

EDA Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN3043548
  • Target Alle Ectodysplasin A (EDA) Antikörper anzeigen
    Ectodysplasin A (EDA)
    Bindungsspezifität
    • 16
    • 16
    • 9
    • 8
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 30-391
    Reaktivität
    • 71
    • 47
    • 28
    • 11
    • 7
    • 7
    • 7
    • 7
    • 6
    • 6
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Human
    Wirt
    • 65
    • 7
    Kaninchen
    Klonalität
    • 64
    • 7
    • 1
    Polyklonal
    Konjugat
    • 27
    • 5
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Dieser Ectodysplasin A Antikörper ist unkonjugiert
    Applikation
    • 67
    • 37
    • 27
    • 26
    • 26
    • 15
    • 11
    • 6
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Verwendungszweck
    Rabbit IgG polyclonal antibody for Ectodysplasin-A(EDA) detection. Tested with WB in Human.
    Kreuzreaktivität (Details)
    No cross reactivity with other proteins.
    Produktmerkmale
    Rabbit IgG polyclonal antibody for Ectodysplasin-A(EDA) detection. Tested with WB in Human.
    Gene Name: ectodysplasin A
    Protein Name: Ectodysplasin-A
    Aufreinigung
    Immunogen affinity purified.
    Immunogen
    E.coli-derived human EDA recombinant protein (Position: A30-S391). Human EDA shares 95% amino acid (aa) sequence identity with mouse EDA.
    Isotyp
    IgG
    Top Product
    Discover our top product EDA Primärantikörper
  • Applikationshinweise
    WB: Concentration: 0.1-0.5 μg/mL, Tested Species: Human, The detection limit for EDA is approximately 0.25 ng/lane under reducing conditions.
    Notes: Tested Species: Species with positive results.
    Other applications have not been tested. Optimal dilutions should be determined by end users.
    Kommentare

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
    Konzentration
    500 μg/mL
    Buffer
    Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Sodium azide.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handhabung
    Avoid repeated freezing and thawing.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    At -20°C for one year. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20 °C for a longer time. Avoid repeated freezing and thawing.
  • Ning, Chen, Li, Wu, Wu, Li, Feng: "X-irradiation for inhibiting glial scar formation in injured spinal cord." in: Neural regeneration research, Vol. 8, Issue 17, pp. 1582-9, (2014) (PubMed).

  • Target
    Ectodysplasin A (EDA)
    Andere Bezeichnung
    EDA (EDA Produkte)
    Synonyme
    ECTD1 antikoerper, ED1 antikoerper, ED1-A1 antikoerper, ED1-A2 antikoerper, EDA-A1 antikoerper, EDA-A2 antikoerper, EDA1 antikoerper, EDA2 antikoerper, HED antikoerper, HED1 antikoerper, ODT1 antikoerper, STHAGX1 antikoerper, XHED antikoerper, XLHED antikoerper, si:ch73-223d24.5 antikoerper, Ed1 antikoerper, Eda-A1 antikoerper, Eda-A2 antikoerper, Ta antikoerper, tabby antikoerper, RGD1563178 antikoerper, ectodysplasin A antikoerper, ectodysplasin-A antikoerper, EDA antikoerper, eda antikoerper, Eda antikoerper
    Hintergrund
    Ectodysplasin-A is a protein that in humans is encoded by the EDA gene. It is mapped to Xq13.1. The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia.

    Synonyms: ECTD1 antibody|Ectodermal dysplasia 1, anhidrotic antibody|Ectodermal dysplasia protein antibody|Ectodermal dysplasia, anhidrotic (hypohydrotic) antibody|Ectodysplasin A antibody|Ectodysplasin A, membrane form antibody|Ectodysplasin A, secreted form antibody|ECTODYSPLASIN A1 ISOFORM antibody|ECTODYSPLASIN A2 ISOFORM antibody|ECTODYSPLASIN antibody|Ectodysplasin-A antibody|ED1 A1 antibody|ED1 A2 antibody|ED1 antibody|ED1 GENE antibody|Eda A1 antibody|Eda A2 antibody|eda antibody|EDA protein antibody|EDA protein homolog antibody|EDA_HUMAN antibody|EDA1 antibody|EDA1 GENE antibody|EDA2 antibody|HED antibody|HED1 antibody|ODT1 antibody|Oligodontia 1 antibody|secreted form antibody|STHAGX1 antibody|Ta antibody|Tabby antibody|Tabby protein antibody|X linked anhidroitic ectodermal dysplasia protein antibody|XHED antibody|XLHED antibody
    Gen-ID
    1896
    UniProt
    Q92838
    Pathways
    Tube Formation
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