- Phare
- Validé par KD/KO
Anticorps Polyclonal de lapin anti-FOXC1
FOXC1 Polyclonal Antibody for IP, WB,ELISA
Hôte / Isotype
Lapin / IgG
Réactivité testée
Humain, souris
Applications
WB, IP, IHC, IF, CoIP, ELISA
Conjugaison
Non conjugué
N° de cat : 55365-1-AP
Synonymes
Galerie de données de validation
Applications testées
Résultats positifs en WB | cellules MCF-7, cellules HEK-293, cellules HepG2 |
Résultats positifs en IP | cellules HepG2, |
Dilution recommandée
Application | Dilution |
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Western Blot (WB) | WB : 1:200-1:1000 |
Immunoprécipitation (IP) | IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate |
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 |
Applications publiées
KD/KO | See 3 publications below |
WB | See 4 publications below |
IHC | See 2 publications below |
IF | See 1 publications below |
CoIP | See 1 publications below |
Informations sur le produit
55365-1-AP cible FOXC1 dans les applications de WB, IP, IHC, IF, CoIP, ELISA et montre une réactivité avec des échantillons Humain, souris
Réactivité | Humain, souris |
Réactivité citée | Humain |
Hôte / Isotype | Lapin / IgG |
Clonalité | Polyclonal |
Type | Anticorps |
Immunogène | Peptide |
Nom complet | forkhead box C1 |
Masse moléculaire calculée | 57 kDa |
Poids moléculaire observé | 70 kDa |
Numéro d’acquisition GenBank | NM_001453 |
Symbole du gène | FOXC1 |
Identification du gène (NCBI) | 2296 |
Conjugaison | Non conjugué |
Forme | Liquide |
Méthode de purification | Purification par affinité contre l'antigène |
Tampon de stockage | PBS avec azoture de sodium à 0,02 % et glycérol à 50 % pH 7,3 |
Conditions de stockage | Stocker à -20 ℃. L'aliquotage n'est pas nécessaire pour le stockage à -20oC Les 20ul contiennent 0,1% de BSA. |
Informations générales
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. This antibody is specific to FOXC1. Phosphorylation modification of Foxc1 protein may be responsible for the larger molecular weight of detection compared with theoretical molecular weight (PMID:27708239;16403239).
Protocole
Product Specific Protocols | |
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WB protocol for FOXC1 antibody 55365-1-AP | Download protocol |
IP protocol for FOXC1 antibody 55365-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |
Publications
Species | Application | Title |
---|---|---|
Bone The osteoporosis risk variant rs9820407 at 3p22.1 acts as an allele-specific enhancer to regulate CTNNB1 expression by long-range chromatin loop formation.
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Tumour Biol The long noncoding RNA FOXCUT promotes proliferation and migration by targeting FOXC1 in nasopharyngeal carcinoma.
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Mol Med Rep FOXC1 silencing inhibits the epithelial‑to‑mesenchymal transition of glioma cells: Involvement of β‑catenin signaling.
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Phytomedicine Icaritin inhibits endometrial carcinoma cells by suppressing O-GlcNAcylation of FOXC1 | ||
J Oral Pathol Med Single-cell RNA sequencing reveals tumor heterogeneity within salivary gland pleomorphic adenoma: A preliminary study |
Avis
The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.
FH Sarah (Verified Customer) (08-20-2021) | I was sent 4 antibodies to try. You can see that JUN (1:1000) and NFKB1 (1:1000) worked, but FOXC1 (1:300) and HES1 (1:500) did not. I have shown that the cells express the mRNA for these proteins by qPCR.
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