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FOXC1 Monoclonal antibody

FOXC1 Monoclonal Antibody for WB, ELISA

Host / Isotype

Mouse / IgG1

Reactivity

human

Applications

WB, ELISA

Conjugate

Unconjugated

CloneNo.

1F4E11

Cat no : 66568-1-Ig

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Synonyms

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



经过测试的应用

Positive WB detected inHeLa cells, HEK-293 cells, HEK293 cells, L02 cells, HepG2 cells

推荐稀释比

ApplicationDilution
Western Blot (WB)WB : 1:2000-1:20000
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.

产品信息

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

Tested Applications WB, ELISA Application Description
Tested Reactivity human
Immunogen Peptide 种属同源性预测
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Full Name forkhead box C1
Synonyms FREAC 3, Forkhead-related transcription factor 3, Forkhead-related protein FKHL7, FKHL7, ARA
Calculated Molecular Weight 57 kDa
Observed Molecular Weight 70-75 kDa
GenBank Accession NumberNM_001453
Gene Symbol FOXC1
Gene ID (NCBI) 2296
RRIDAB_2881929
Conjugate Unconjugated
Form Liquid
Purification MethodProtein G purification
UNIPROT IDQ12948
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

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.

实验方案

Product Specific Protocols
WB protocol for FOXC1 antibody 66568-1-IgDownload protocol
Standard Protocols
Click here to view our Standard Protocols