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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
Synonyms
Validation Data Gallery
Tested Applications
Positive WB detected in | HeLa cells, HEK-293 cells, HEK293 cells, L02 cells, HepG2 cells |
Recommended dilution
Application | Dilution |
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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. |
Product Information
66568-1-Ig targets FOXC1 in WB, ELISA applications and shows reactivity with human samples.
Tested Reactivity | human |
Host / Isotype | Mouse / IgG1 |
Class | Monoclonal |
Type | Antibody |
Immunogen | Peptide 相同性解析による交差性が予測される生物種 |
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 |
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 -20oC storage. |
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.
Protocols
Product Specific Protocols | |
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WB protocol for FOXC1 antibody 66568-1-Ig | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |