FOXI1 antibody
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- Target See all FOXI1 Antibodies
- FOXI1 (Forkhead Box I1 (FOXI1))
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This FOXI1 antibody is un-conjugated
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Characteristics
- Polyclonal Antibody
- Purification
- Antigen affinity purification
- Immunogen
- Synthetic peptide of human FOXI1
- Isotype
- IgG
- Top Product
- Discover our top product FOXI1 Primary Antibody
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- Application Notes
- WB 1:500-1:2000, IHC 1:50-1:200, ELISA 1:5000-1:10000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1.62 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- FOXI1 (Forkhead Box I1 (FOXI1))
- Alternative Name
- FOXI1 (FOXI1 Products)
- Synonyms
- FKH10 antibody, FKHL10 antibody, FREAC-6 antibody, FREAC6 antibody, HFH-3 antibody, HFH3 antibody, 5830401E05Rik antibody, Fkh10 antibody, Hfh3 antibody, cb724 antibody, foo antibody, Xfoxi1a antibody, ema antibody, foxi1a antibody, foxi1e antibody, xema antibody, xfoxi1 antibody, FoxI1e antibody, Xema antibody, fkhl10 antibody, freac6 antibody, hfh3 antibody, FOXI1 antibody, forkhead box I1 antibody, forkhead box i1 antibody, forkhead box I1 L homeolog antibody, forkhead box protein I1 antibody, FOXI1 antibody, Foxi1 antibody, foxi1 antibody, foxi1.L antibody, CC1G_14832 antibody
- Background
- This gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene may play an important role in the development of the cochlea and vestibulum, as well as in embryogenesis. The encoded protein has been found to be required for the transcription of four subunits of a proton pump found in the inner ear, the kidney, and the epididymis. Mutations in this gene have been associated with deafness, autosomal recessive 4.
- Molecular Weight
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Observed_MW: Refer to figures
Calculated_MW: 41 kDa
- UniProt
- Q12951
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