FOXC1 Rabbit Polyclonal Antibody (CAB2924)
- SKU:
- CAB2924
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cardiovascular
Frequently bought together:
Description
Product Name: | FOXC1 Rabbit Polyclonal Antibody |
SKU: | CAB2924 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 404-553 of human FOXC1 (NP_001444.2). |
Sequence: | AAGE RGGH LQGA PGGA GGSA VDDP LPDY SLPP VTSS SSSS LSHG GGGG GGGG GQEA GHHP AAHQ GRLT SWYL NQAG GDLG HLAS AAAA AAAA GYPG QQQN FHSV REMF ESQR IGLN NSPV NGNS SCQM AFPS SQSL YRTS GAFV YDCS KF |
Tested Applications: | WB ELISA |
Recommended Dilution: | WB,1:100 - 1:1000 |
Synonyms: | ARA; IGDA; IHG1; ASGD3; FKHL7; IRID1; RIEG3; FREAC3; FREAC-3; FOXC1 |
Positive Sample: | HeLa,Jurkat,SKOV3,Mouse kidney,Mouse lung,Rat brain |
Conjugate: | Unconjugated |
Cellular Localization: | Nucleus. |
Calculated MW: | 57kDa |
Observed MW: | 70kDa |
This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.
Purification Method: | Affinity purification |
Gene ID: | 2296 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3. |