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ALDOA Antikörper (N-Term)

Dieser Anti-ALDOA Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von ALDOA in WB. Geeignet für Human, Maus, Ratte, Kaninchen, Hund, Rind (Kuh), Meerschweinchen, Pferd, Zebrafisch (Danio rerio) und Schaf. Dieses Primary Antibody wurde in 2+ Publikationen zitiert.
Produktnummer ABIN2783231

Kurzübersicht für ALDOA Antikörper (N-Term) (ABIN2783231)

Target

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

Reaktivität

  • 80
  • 31
  • 28
  • 16
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte, Kaninchen, Hund, Rind (Kuh), Meerschweinchen, Pferd, Zebrafisch (Danio rerio), Schaf

Wirt

  • 60
  • 12
  • 12
  • 2
Kaninchen

Klonalität

  • 70
  • 15
Polyklonal

Konjugat

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

Applikation

  • 68
  • 41
  • 25
  • 22
  • 16
  • 11
  • 9
  • 7
  • 6
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 10
    • 6
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Sequenz

    MPYQYPALTP EQKKELSDIA HRIVAPGKGI LAADESTGSI AKRLQSIGTE

    Homologie

    Cow: 93%, Dog: 100%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Mouse: 92%, Rabbit: 100%, Rat: 93%, Sheep: 82%, Zebrafish: 92%

    Produktmerkmale

    This is a rabbit polyclonal antibody against ALDOA. It was validated on Western Blot using a cell lysate as a positive control.

    Aufreinigung

    Protein A purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N terminal region of human ALDOA
  • Applikationshinweise

    Optimal working dilutions should be determined experimentally by the investigator.

    Kommentare

    Antigen size: 364 AA

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    Lot specific

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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 freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Braceland, McLoughlin, Tinsley, Wallace, Cockerill, McLaughlin, Eckersall: "Serum enolase: a non-destructive biomarker of white skeletal myopathy during pancreas disease (PD) in Atlantic salmon Salmo salar L." in: Journal of fish diseases, Vol. 38, Issue 9, pp. 821-31, (2015) (PubMed).

    Mao, Yang, Xu, Sang, Lu, Yang, Zhang, Zhong, Huang, Zhang: "[Significance of Golgi glycoprotein 73, a new tumor marker in diagnosis of hepatocellular carcinoma: a primary study]." in: Zhonghua yi xue za zhi, Vol. 88, Issue 14, pp. 948-51, (2008) (PubMed).

  • Target

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

    Andere Bezeichnung

    ALDOA

    Hintergrund

    ALDOA is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. 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.This gene product, 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 of this gene results in multiple transcript variants which encode the same protein.
    Alias Symbols: ALDA, MGC10942, MGC17716, MGC17767, GSD12
    Protein Interaction Partner: HUWE1, UBC, IFNA4, FUS, ALDOC, ALDOA, SUMO2, SUMO3, MDM2, ADRB2, SUZ12, TNPO3, CS, RAD52, VCPKMT, PIAS4, GALNT6, IQCB1, VCAM1, MLH1, ITGA4, HSP90AB1, HSP90AA1, FN1, ATF2, BCAT2, ALDOB, LIG4, PGK1, LGALS1, HSPD1, AKT1, MYOC, CDK2, CUL2, CUL3, CUL4B, ISG15,
    Protein Size: 364

    Molekulargewicht

    39 kDa

    Gen-ID

    226

    NCBI Accession

    NM_000034, NP_000025

    UniProt

    P04075

    Pathways

    Ribonucleoside Biosynthetic Process
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