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ALDOA Antikörper

Dieses Anti-ALDOA-Antikörper ist ein Kaninchen Monoklonal-Antikörper zur Detektion von ALDOA in WB und IHC. Geeignet für Human.
Produktnummer ABIN7265550

Kurzübersicht für ALDOA Antikörper (ABIN7265550)

Target

Alle ALDOA Antikörper anzeigen
ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

Reaktivität

  • 81
  • 32
  • 30
  • 17
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 60
  • 14
  • 12
  • 2
Kaninchen

Klonalität

  • 71
  • 16
Monoklonal

Konjugat

  • 59
  • 7
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Dieser ALDOA Antikörper ist unkonjugiert

Applikation

  • 70
  • 41
  • 26
  • 22
  • 18
  • 13
  • 9
  • 7
  • 6
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Verwendungszweck

    ALDOA Rabbit mAb

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human Aldolase

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

    Andere Bezeichnung

    ALDOA

    Hintergrund

    The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10. [provided by RefSeq, Aug 2011],ALDA, GSD12, HEL-S-87p,Amino acid metabolism,Cancer,Carbohydrate metabolism,Cell Biology & Developmental Biology,Cell Cycle,Cell Cycle_Centrosome,Endocrine & Metabolism,Signal Transduction,ALDOA

    Molekulargewicht

    39kDa

    Gen-ID

    226

    UniProt

    P04075

    Pathways

    Ribonucleoside Biosynthetic Process
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