FOXE3 antibody (AA 87-114)

Catalog No. ABIN5531185

Product Details anti-FOXE3 Antibody

Target: FOXE3 (Forkhead Box E3 (FOXE3))

Binding Specificity: AA 87-114

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FOXE3 antibody is un-conjugated

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This FOXE3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 87-114 amino acids from the Central region of human FOXE3.

Isotype: Ig Fraction

Application Details

Application Notes: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details for FOXE3

Target: FOXE3 (Forkhead Box E3 (FOXE3))

Alternative Name: FOXE3 (FOXE3 Products)

Synonyms: FOXE3 antibody, FKHL12 antibody, FREAC8 antibody, dyl antibody, rct antibody, FREAC-8 antibody, HFH7 antibody, HNF3 antibody, foxe4 antibody, lens1 antibody, lens1-A antibody, forkhead box E3 antibody, forkhead box E3 L homeolog antibody, foxe3 antibody, FOXE3 antibody, LOC100301611 antibody, Foxe3 antibody, foxe3.L antibody

Background: This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. The protein encoded functions as a lens-specific transcription factor and plays an important role in vertebrate lens formation. Mutations in this gene are associated with anterior segment mesenchymal dysgenesis and congenital primary aphakia.

Molecular Weight: 33 kDa

Gene ID: 2301

UniProt: Q13461