PIPA530190

NR2F1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA530190-Each-of-1 In Stock ₹ 46,502.50

PIPA530190 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

NR2F1

Classification

Polyclonal

Conjugate

Unconjugated

Gene

Nr2f1

Gene Alias

avian erythroblastic leukemia viral (v-erb-a) oncogene homolog-like 3; BBOAS; BBSOAS; chicken ovalbumin upstream promoter-transcription factor I; COUP transcription factor 1; COUP transcription factor I; COUP-TF I; COUP-TF1; COUPTFA; COUP-TFI; EAR3; EAR-3; Erbal3; Nr2f1; NR2F2; Nuclear receptor subfamily 2 group F member 1; nuclear receptor subfamily 2, group F, member 1; SVP44; Tcfcoup1; TFCOUP1; transcription factor COUP 1 (chicken ovalbumin upstream promoter 1, v-erb-a homolog-like 3); V-erbA-related protein 3

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

7025

Content And Storage

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

Form

Liquid

Applications

ChIP Assay, Immunoprecipitation, Western Blot

Concentration

0.92 mg/mL

Formulation

0.1M tris glycine with 20% glycerol and 0.01% thimerosal; pH 7

Gene Accession No.

P10589

Gene Symbols

Nr2f1

Immunogen

Recombinant fragment corresponding to a region within amino acids 163 and 423 of Human COUP TF1

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

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Description

  • Recommended positive controls: A549, HeLa, HCT116
  • Predicted reactivity: Mouse (100%), Rat (99%), Xenopus laevis (98%), Bovine (100%)
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • The protein encoded by this gene is a nuclear hormone receptor and transcriptional regulator
  • The encoded protein acts as a homodimer and binds to 5'-AGGTCA-3' repeats
  • Defects in this gene are a cause of Bosch-Boonstra optic atrophy syndrome (BBOAS).