FOXG1 Recombinant antibody

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  WB analysis using 85930-1-RR

  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.

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  IF Staining of C6 using 85930-1-RR

  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).

FOXG1 Uni-rAb^TM Recombinant Antibody for WB, IF/ICC, ELISA

Cat No. 85930-1-RR

Clone No.250144E8

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IF/ICC, ELISA

Synonyms

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

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Tested Applications

• Positive WB detected in: mouse brain tissue, rat brain tissue
• Positive IF/ICC detected in: C6 cells

Recommended dilution

• Western Blot (WB): WB : 1:5000-1:50000
• Immunofluorescence (IF)/ICC: IF/ICC : 1:400-1:1600

It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Sample-dependent, Check data in validation data gallery.

Product Information

85930-1-RR targets FOXG1 in WB, IF/ICC, ELISA applications and shows reactivity with human, mouse, rat samples.

• Tested Reactivity: human, mouse, rat
• Host / Isotype: Rabbit / IgG
• Class: Recombinant
• Type: Antibody
• Immunogen: FOXG1 fusion protein Ag17169
• Full Name: forkhead box G1
• Calculated Molecular Weight: 489 aa, 52 kDa
• GenBank Accession Number: BC035020
• Gene Symbol: FOXG1
• Gene ID (NCBI): 2290
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Protein A purification
• UNIPROT ID: P55316
• Storage Buffer: PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
• Storage Conditions: Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20^oC storage. 20ul sizes contain 0.1% BSA.

Background Information

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.