PIPA527143

FOXE1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA527143-Each-of-1 In Stock ₹ 45,968.50

PIPA527143 - Each of 1

₹ 45,968.50

In Stock

Quantity

1

Base Price: ₹ 45,968.50

GST (18%): ₹ 8,274.33

Total Price: ₹ 54,242.83

Antigen

FOXE1

Classification

Polyclonal

Conjugate

Unconjugated

Gene

FOXE1

Gene Alias

FKHL15; forkhead box E1; forkhead box E1 (thyroid transcription factor 2); forkhead box E2; forkhead box protein E1; Forkhead box protein E2; forkhead, drosophila, homolog-like 15; forkhead-related protein FKHL15; Foxe1; FOXE2; HFKH4; HFKL5; HNF-3/fork head-like protein 5; NMTC4; Thyroid transcription factor 2; Titf2; TTF2; TTF-2

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

2304

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

Immunoprecipitation, Western Blot

Concentration

1 mg/mL

Formulation

PBS with 20% glycerol and 0.01% thimerosal; pH 7

Gene Accession No.

O00358

Gene Symbols

FOXE1

Immunogen

Synthetic peptide corresponding to a region within amino acids 311 and 373 of FOXE1

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PIPA527142

--

Img

Thermo Scientific

PIPA527145

--

Img

Thermo Scientific

PIPA527157

--

Img

Thermo Scientific

PIPA521385

--

Img

Thermo Scientific

PIPA520973

--

Img

Thermo Scientific

PIPA527243

--

Img

Thermo Scientific

PIPA527158

--

Img

Thermo Scientific

PIPA527365

--

Description

  • Recommended positive controls: HeLaS3
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain
  • This gene functions as a thyroid transcription factor which likely plays a crucial role in thyroid morphogenesis
  • Mutations in this gene are associated with congenital hypothyroidism and cleft palate with thyroid dysgenesis
  • The map localization of this gene suggests it may also be a candidate gene for squamous cell epithelioma and hereditary sensory neuropathy type I.