PA548328

TGIF Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PA548328-Each-of-1 In Stock ₹ 46,502.50

PA548328 - 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

TGIF

Classification

Polyclonal

Conjugate

Unconjugated

Gene

TGIF1

Gene Alias

5'-TG-3'-interacting factor 1; AA959811; AI462167; Homeobox protein TGIF1; HPE4; TALE family homeobox; TALE homeobox TG-interacting factor; Tfig; TG interacting factor 1; TGFB induced factor homeobox 1; TGFB-induced factor homeobox 1; TGIF; Tgif1; transforming growth factor-beta-induced factor

Host Species

Rabbit

Purification Method

Ammonium sulfate precipitation

Regulatory Status

RUO

Gene ID (Entrez)

21815, 7050

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

Western Blot

Concentration

2.0 mg/mL

Formulation

PBS with 0.09% sodium azide

Gene Accession No.

P70284, Q15583

Gene Symbols

TGIF1

Immunogen

KLH conjugated synthetic peptide between 208-237 amino acids from the Central region of human TGIF1.

Quantity

400 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

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Description

  • Predicted to react with chicken based on sequence homology
  • TGIF is a member of the three-amino acid loop extension (TALE) superclass of atypical homeodomains
  • TALE homeobox proteins are highly conserved transcription regulators
  • This particular homeodomain binds to a previously characterized retinoid X receptor responsive element from the cellular retinol-binding protein II promoter
  • In addition to its role in inhibiting 9-cis-retinoic acid-dependent RXR alpha transcription activation of the retinoic acid responsive element, the protein is an active transcriptional co-repressor of SMAD2 and may participate in the transmission of nuclear signals during development and in the adult
  • Mutations in this gene are associated with holoprosencephaly type 4, which is a structural anomaly of the brain.