18-022-1

Nkx2.1 Monoclonal Antibody (8G7G3/1), Invitrogen™

Manufacturer: Invitrogen

Select a Size

Pack Size SKU Availability Price
Each 18-022-1-Each In Stock ₹ 45,091.85

18-022-1 - Each

₹ 45,091.85

In Stock

Quantity

1

Base Price: ₹ 45,091.85

GST (18%): ₹ 8,116.533

Total Price: ₹ 53,208.383

Antigen

Nkx2.1

Classification

Monoclonal

Conjugate

Unconjugated

Gene

NKX2-1

Gene Alias

AV026640; BCH; BHC; homeobox protein NK-2 homolog A; Homeobox protein Nkx-2.1; NK-2; NK2 homeobox 1; NK-2 homolog A; NKX2.1; Nkx-2.1; NKX2-1; NKX2A; NMTC1; RNA polymerase I transcription termination factor; T/EBP; TEBP; Thyroid nuclear factor 1; thyroid transcription factor 1; thyroid transcription factor 1 TTF-1 NK-2; thyroid transcription factor 1-like; thyroid-specific enhancer-binding protein; tinman; TITF1; TTF1; TTF-1

Host Species

Mouse

Purification Method

purified

Regulatory Status

RUO

Gene ID (Entrez)

7080

Content And Storage

2-8°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin)

Clone

8G7G3/1

Formulation

PBS with 1% BSA and 0.1% sodium azide

Gene Accession No.

P43699

Gene Symbols

NKX2-1

Immunogen

Recombinant full length TTF-1 (Thyroid Transcription Factor 1) protein

Quantity

1 mL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

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Description

  • TTF-1 has been identified as a mediator of thyroid-specific gene transcription, and is involved in the activation of pulmonary-specific genes
  • TTF-1 is found in primary lung adenocarcinomas and small cell carcinomas
  • TTF-1 is usually absent in breast and colon carcinomas
  • TTF-1 monoclonal antibody should be useful in differentiating tumors of lung and non-lung origin
  • Lung cancer and thyroid gland tissues have been identified positive for TTF-1 monoclonal antibody concentrate
  • This gene encodes a protein initially identified as a thyroid-specific transcription factor
  • The encoded protein binds to thyroglobulin promoter and regulates the expression of thyroid-specific genes but has also been shown to regulate the expression of genes involved in morphogenesis
  • Mutations and deletions in this gene are associated with benign hereditary chorea, choreoathetosis, congenital hypothyroidism, and neonatal respiratory distress, and may be associated with thyroid cancer
  • Multiple transcript variants encoding different isoforms have been found for this gene.