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Anti-FOXC1 Antibody (clone 4D11) LS-C197229

Ordering

Wt. Vol. Conc. Price
100 µg - - $355
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)
206-374-1102
866-206-6909
Orders@LSBio.com
 

Most Popular FOXC1 Antibodies

Anti-FOXC1 Antibody (aa250-300) IHC-plus™ LS-B1800
Rabbit Polyclonal to Human FOXC1
Human, Monkey, Mouse, Rat, Bovine
IHC - Paraffin, Western blot
Unconjugated
Immunohistochemistry Image
Anti-FOXC1 Antibody (aa541-553) IHC-plus™ LS-B2996
Goat Polyclonal to Human FOXC1
Human, Monkey, Mouse, Xenopus, Zebrafish
IHC - Paraffin, Western blot, ELISA
Unconjugated
Immunohistochemistry Image
Anti-FOXC1 Antibody (aa35-84) IHC-plus™ LS-B4579
Rabbit Polyclonal to Human FOXC1
Human, Monkey, Rat, Zebrafish
IHC - Paraffin, Western blot
Unconjugated
Immunohistochemistry Image

100% Guaranteed 100% Guaranteed
Mouse Monoclonal [clone 4D11] (IgG2b,k) to Human FOXC1
Human
Western blot, ELISA
Unconjugated

Details

Human FOXC1
Mouse
Human (tested or 100% immunogen sequence identity)
IgG2b,k Monoclonal [4D11]
Unconjugated
Protein A purified
Unmodified

Applications

  • Western blot
  • ELISA

Specificity and Use

FOXC1 antibody was raised against fOXC1 (NP_001444, aa464-553 full length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Human FOXC1
Western Blot: Recombinant protein.

Packaging

PBS, pH 7.2
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
For research use only.

About FOXC1

Q12948 NM_001453 NP_001444.2

FOXC1 Antibody, Forkhead-like 7 Antibody, FREAC3 Antibody, FKHL7 Antibody, Forkhead-related activator 3 Antibody, Forkhead-related protein FKHL7 Antibody, IGDA Antibody, IHG1 Antibody, IRID1 Antibody, Forkhead box protein C1 Antibody, Mesenchyme fork head protein 1 Antibody, Myeloid factor-delta Antibody, ARA Antibody, Forkhead box C1 Antibody, FREAC-3 Antibody, RIEG3 Antibody

Forkhead box C1 (FOXC1) belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of FOXC1 has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in FOXC1 cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.

Requested From: United States
Date Requested: 12/10/2016

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