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Aldolase anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-Aldolase a été validé pour WB, IF et IHC (p). Il convient pour détecter Aldolase dans des échantillons de Humain.
N° du produit ABIN5530350

Aperçu rapide pour Aldolase anticorps (N-Term) (ABIN5530350)

Antigène

Voir toutes Aldolase (ALD) Anticorps
Aldolase (ALD)

Reactivité

  • 16
  • 8
  • 8
  • 7
  • 5
Humain

Hôte

  • 16
  • 3
  • 2
Lapin

Clonalité

  • 14
  • 7
Polyclonal

Conjugué

  • 8
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Aldolase est non-conjugé

Application

  • 14
  • 11
  • 10
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Épitope

    • 2
    • 1
    • 1
    AA 66-95, N-Term

    Purification

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis

    Immunogène

    This Aldolase (ALDOA) antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 66-95 amino acids from the N-terminal region of human Aldolase (ALDOA).

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    For IHC-P starting dilution is: 1:10~50

    For IF starting dilution is: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    2 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène

    Aldolase (ALD)

    Autre désignation

    Aldolase

    Sujet

    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.

    Poids moléculaire

    39 kDa

    ID gène

    226

    UniProt

    P04075
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