ARG43937

anti-OVOL2 antibody

anti-OVOL2 antibody for ELISA,Flow cytometry,ICC/IF,Western blot and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes OVOL2
Tested Reactivity Hu
Tested Application ELISA, FACS, ICC/IF, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name OVOL2
Antigen Species Human
Immunogen Human OVOL2 recombinant protein
Expression System E.coli
Conjugation Un-conjugated
Protein Full Name Transcription factor Ovo-like 2
Alternate Names OVOL2; Ovo Like Zinc Finger 2; Zinc Finger Protein 339; ZNF339; CHED; Corneal Endothelial Dystrophy 1 (Autosomal Dominant); Transcription Factor Ovo-Like 2; BA504H3.3; HOVO2; CHED1; Ovo-Like 2 (Drosophila); EUROIMAGE566589; CHED2; PPCD1; HOvo2

Application Instructions

Application Suggestion
Tested Application Dilution
ELISA0.1-0.5 µg/ml
FACS1-3 µg/1x10^6 cells
ICC/IF5 µg/ml
WB0.25-0.5 µg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Affinity purified with Immunogen.
Buffer 0.9% NaCl, 0.2% Na2HPO4 and 4% Trehalose.
Stabilizer 4% Trehalose
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 58495 Human OVOL2

Swiss-port # Q9BRP0 Human Transcription factor Ovo-like 2

Gene Symbol OVOL2
Gene Full Name Ovo Like Zinc Finger 2
Background This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy.
Function Plays dual functions in thermogenesis and adipogenesis to maintain energy balance. Essential for brown/beige adipose tissue-mediated thermogenesis, is necessary for the development of brown adipocytes. In white adipose tissues, limits adipogenesis by blocking CEBPA binding to its transcriptional targets and inhibiting its transcription factor activity.
Cellular Localization Nucleus
Calculated MW 30 kDa
PTM Phosphoprotein