FOXI1 antibody (N-Term)

Catalog No. ABIN2780863

Product Details anti-FOXI1 Antibody

Target: FOXI1 (Forkhead Box I1 (FOXI1))

Binding Specificity: N-Term

Reactivity: Human, Mouse, Guinea Pig, Rat, Cow, Rabbit, Dog

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FOXI1 antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: MSSFDLPAPS PPRCSPQFPS IGQEPPEMNL YYENFFHPQG VPSPQRPSFE

Predicted Reactivity: Cow: 100%, Dog: 93%, Guinea Pig: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%

Characteristics: This is a rabbit polyclonal antibody against FOXI1. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N terminal region of human FOXI1

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator.

Comment:

Antigen size: 378 AA

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freeze-thaw cycles.

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for FOXI1

Target: FOXI1 (Forkhead Box I1 (FOXI1))

Alternative Name: FOXI1 (FOXI1 Products)

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.
Alias Symbols: FKHL10, FREAC6, HFH3, MGC34197, FKH10, HFH-3, FREAC-6
Protein Interaction Partner: APP, COPS6,
Protein Size: 378

Molecular Weight: 41 kDa

Gene ID: 2299

NCBI Accession: NM_012188, NP_036320

UniProt: Q12951