Anticorps Recombinant de lapin anti-FOXG1

FOXG1 Recombinant Antibody for WB, IF/ICC, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, rat, souris

Applications

WB, IF/ICC, Indirect ELISA

Conjugaison

Non conjugué

CloneNo.

250144E8

N° de cat : 85930-1-PBS

Synonymes

FOXG 1, BF-1, BF-2, forkhead box G1, Forkhead box protein G1

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Galerie de données de validation

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  WB analysis using 85930-1-RR (same clone as 85930-1-PBS)

  Various lysates were subjected to SDS PAGE followed by western blot with 85930-1-RR (FOXG1 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 85930-1-PBS in a different storage buffer formulation.

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  IF Staining of C6 using 85930-1-RR (same clone as 85930-1-PBS)

  Immunofluorescent analysis of (4% PFA) fixed C6 cells using FOXG1 antibody (85930-1-RR, Clone: 250144E8 ) at dilution of 1:800 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red). This data was developed using the same antibody clone with 85930-1-PBS in a different storage buffer formulation.

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Informations sur le produit

85930-1-PBS cible FOXG1 dans les applications de WB, IF/ICC, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat, souris

• Réactivité: Humain, rat, souris
• Hôte / Isotype: Lapin / IgG
• Clonalité: Recombinant
• Type: Anticorps
• Immunogène: FOXG1 Protéine recombinante Ag17169
• Nom complet: forkhead box G1
• Masse moléculaire calculée: 489 aa, 52 kDa
• Poids moléculaire observé: 60 kDa
• Numéro d’acquisition GenBank: BC035020
• Symbole du gène: FOXG1
• Identification du gène (NCBI): 2290
• Conjugaison: Non conjugué
• Forme: Liquide
• Méthode de purification: Purification par protéine A
• Tampon de stockage: PBS only
• Conditions de stockage: Store at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

Forkhead Box G1 (FOXG1) is a member of the Forkhead family of genes with non-redundant roles in brain development, where alteration of this gene's expression significantly affects the formation and function of the mammalian cerebral cortex. FOXG1 haploinsufficiency in humans is associated with prominent differences in brain size and impaired intellectual development noticeable in early childhood, while homozygous mutations are typically fatal.

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