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Antibody used in WB on Human Heart at 0.2-1 ug/ml.
Antibody used in WB on Human Heart at 0.2-1 ug/ml.

FOXI1 Antibody

CATALOG NUMBER: 25-466

Clonality:
Polyclonal
Tested Applications:
ELISA, WB
Host Species:
Rabbit
Species Reactivity:
Human
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FOXI1.
Conjugate:
Unconjugated
Tested Applications:
ELISA, WB
Application Note:
FOXI1 antibody can be used for detection of FOXI1 by ELISA at 1:62500. FOXI1 antibody can be used for detection of FOXI1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
Cat. No. XBL-10407 - Fetal Heart Tissue Lysate
Predicted Molecular Weight:
41 kDa
Purification:
Antibody is purified by peptide affinity chromatography method.
Clonality:
Polyclonal
Physical State:
Liquid
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Storage Conditions:
For short periods of storage (days) store at 4°C. For longer periods of storage, store FOXI1 antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
FOXI1
Additional Names:
FOXI1, FKHL10, FREAC6, HFH3, MGC34197, FKH10, HFH-3, FREAC-6
Protein Accession Number:
NP_036320
Protein Gi Number:
21618327
Ncbi Gene Id Number:
2299
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
FOXI1 belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. FOXI1 may plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis.This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it is possible that this gene plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis. Mutations in this gene may be associated with the common cavity phenotype. Two transcript variants encoding different isoforms have been found for this gene.
Background Reference 1:
Clevidence, D.E., (2003) Mol. Pharmacol. 63 (5), 1180-1189.

FOR RESEARCH USE ONLY

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Disclaimer:
This product is for research use only.

CATALOG NUMBER:

25-466

List Size:
100 ul

List Price:

$519.00

Datasheet
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