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ALDOA Antikörper

Dieser 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

  • 80
  • 32
  • 29
  • 17
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 60
  • 12
  • 12
  • 2
Kaninchen

Klonalität

  • 71
  • 14
Monoklonal

Konjugat

  • 57
  • 7
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Dieser ALDOA Antikörper ist unkonjugiert

Applikation

  • 68
  • 41
  • 24
  • 22
  • 16
  • 11
  • 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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