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FOXG1 Rekombinanter Antikörper

FOXG1 Rekombinant Antikörper für WB, IF/ICC, Indirect ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, IF/ICC, Indirect ELISA

Konjugation

Unkonjugiert

CloneNo.

250144E8

Kat-Nr. : 85930-1-PBS

Synonyme

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

Filter:
  • Western Blot (WB) analysis of various lysates using FOXG1 Recombinant antibody (85930-1-RR)

    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.

  • Immunofluorescence (IF) / fluorescent staining of C6 cells using FOXG1 Recombinant antibody (85930-1-RR)

    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.

Geprüfte Anwendungen

Produktinformation

85930-1-PBS bindet in WB, IF/ICC, Indirect ELISA FOXG1 und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
Wirt / Isotyp Kaninchen / IgG
Klonalität Rekombinant
Typ Antikörper
Immunogen FOXG1 fusion protein Ag17169
Vollständiger Name forkhead box G1
Berechnetes Molekulargewicht 489 aa, 52 kDa
Beobachtetes Molekulargewicht60 kDa
GenBank-ZugangsnummerBC035020
Gene symbol FOXG1
Gene ID (NCBI) 2290
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein-A-Reinigung
Lagerungspuffer PBS only
LagerungsbedingungenStore at -80°C. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

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.