MABE1529MI

MilliporeSigma™ BRD7, Rat, Unlabeled, Clone: BRM203,

Manufacturer: MilliporeSigma™

Select a Size

Pack Size SKU Availability Price
Each of 1 MABE1529MI-Each-of-1 In Stock ₹ 42,968.31

MABE1529MI - Each of 1

₹ 42,968.31

In Stock

Quantity

1

Base Price: ₹ 42,968.31

GST (18%): ₹ 7,734.296

Total Price: ₹ 50,702.606

Antigen

BRD7

Classification

Monoclonal

Concentration

Please refer to lot specific datasheet.

Formulation

Purified rat monoclonal IgG2aκ antibody in buffer containing 0.1M Tris-Glycine (pH 7.4), 150mM NaCl with 0.05% Sodium Azide.

Gene Accession No.

Q9NPI1

Immunogen

Recombinant human BRD7.

Quantity

100 μg

Research Discipline

Epigenetics & Nuclear Function

Gene ID (Entrez)

NP_001167455

Target Species

Human

Form

Purified

Applications

Western Blot

Clone

BRM203

Conjugate

Unconjugated

Gene

BRD7, BP75, CELTIX1

Host Species

Rat

Purification Method

Protein G Purified

Regulatory Status

RUO

Primary or Secondary

Primary

Test Specificity

Clone BRM 2D3 detects human 75 kDa bromodomain protein, also known as protein CELTIX-1.

Content And Storage

Stable for 1 year at 2°-8°C from date of receipt.

Isotype

IgG2a κ

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Description

  • Bromodomain-containing protein 7 (UniProt Q9NPI1; also known as 75kDa bromodomain protein, Protein CELTIX-1) is encoded by the BRD7 (also known as BP75, CELTIX1) gene (Gene ID 29117) in human
  • BRD7 is a ubiquitously expressed single bromodomain-/BRD-containing member of the family of BRD-containing proteins
  • BRD7 functions as a subunit of the SWI/SNF chromatin-remodeling complex involved in transcription regulation
  • It also interacts with the well known tumor suppressor p53 to trans-activate genes involved in cell cycle arrest
  • BRD7 is downregulated in colorectal carcinoma and nasopharyngeal carcinoma, and BRD7 overexpression is reported to inhibit nasopharyngeal carcinoma cell proliferation via cell cycle arrest by transcriptionally regulating ras/MEK/ERK, Rb/E2F, b-catenin and ERK pathways
  • BRD7 mRNA has been identified as a silencing target of miR-300, overexpression of miR-300 promotes the proliferation, invasion and EMT of osteosarcoma cells through targeting BRD7 mRNA.