FOXC1 Monoclonal antibody, PBS Only

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  WB analysis using 66568-1-Ig (same clone as 66568-1-PBS)

  Various cells were subjected to SDS PAGE followed by western blot with 66568-1-Ig (FOXC1 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 66568-1-PBS in a different storage buffer formulation.

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  WB analysis of HEK-293 using 66568-1-Ig (same clone as 66568-1-PBS)

  WB result of FOXC1 antibody (66568-1-Ig; 1:10000; incubated at room temperature for 1.5 hours) with sh-Control and sh-FOXC1 transfected HEK-293 cells. This data was developed using the same antibody clone with 66568-1-PBS in a different storage buffer formulation.

• Featured Product
• KD/KO Validated

FOXC1 Monoclonal Antibody for WB, Indirect ELISA

Cat No. 66568-1-PBS

Clone No.1F4E11

Host / Isotype

Mouse / IgG1

Reactivity

human

Applications

WB, Indirect ELISA

Synonyms

FREAC 3, Forkhead-related transcription factor 3, Forkhead-related protein FKHL7, FKHL7, ARA

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Product Information

66568-1-PBS targets FOXC1 in WB, Indirect ELISA applications and shows reactivity with human samples.

• Tested Reactivity: human
• Host / Isotype: Mouse / IgG1
• Class: Monoclonal
• Type: Antibody
• Immunogen: Peptide
• Full Name: forkhead box C1
• Calculated Molecular Weight: 57 kDa
• Observed Molecular Weight: 70-75 kDa
• GenBank Accession Number: NM_001453
• Gene Symbol: FOXC1
• Gene ID (NCBI): 2296
• RRID: AB_2881929
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Protein G purification
• UNIPROT ID: Q12948
• Storage Buffer: PBS Only
• Storage Conditions: Store at -80°C.

Background Information

FOXC1, also named as FKHL7 and FREAC3, binding of FREAC-3 and FREAC-4 to their cognate sites results in bending of the DNA at an angle of 80-90 degrees. Defects in FOXC1 are the cause of Axenfeld-Rieger syndrome type 3 (RIEG3). Defects in FOXC1 are the cause of iridogoniodysgenesis anomaly (IGDA). Defects in FOXC1 are a cause of Peters anomaly.