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Anticorps Polyclonal de lapin anti-HBG2

HBG2 Polyclonal Antibody for WB, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain

Applications

WB, Indirect ELISA

Conjugaison

Non conjugué

N° de cat : 31753-1-PBS

Synonymes

Galerie de données de validation

Filter:
  • Western Blot (WB) analysis of various lysates using HBG2 Polyclonal antibody (31753-1-AP)

    WB analysis using 31753-1-AP (same clone as 31753-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 31753-1-AP (HBG2 antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 31753-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of various lysates using HBG2 Polyclonal antibody (31753-1-AP)

    WB analysis using 31753-1-AP (same clone as 31753-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 31753-1-AP (HBG2 antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 31753-1-PBS in a different storage buffer formulation.

Informations sur le produit

31753-1-PBS cible HBG2 dans les applications de WB, Indirect ELISA et montre une réactivité avec des échantillons Humain

Réactivité Humain
Hôte / Isotype Lapin / IgG
Clonalité Polyclonal
Type Anticorps
Immunogène HBG2 Protéine recombinante Ag36028
Nom complet hemoglobin, gamma G
Masse moléculaire calculée 16 kDa
Poids moléculaire observé14~16 kDa
Numéro d’acquisition GenBankBC029387
Symbole du gène HBG2
Identification du gène (NCBI) 3048
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par affinité contre l'antigène
Tampon de stockage PBS only
Conditions de stockageStore at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

The gamma globin genes (HBG2, encoding Gγ-globin; HBG1 encoding Aγ-globin) are normally expressed in the fetal liver, spleen and bone marrow. Two gamma chains together with two alpha chains constitute fetal hemoglobin (HbF) which is normally replaced by adult hemoglobin (HbA) at birth. Gamma chain production continues into adulthood in some beta-thalassemias and related conditions.

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