BDB563593

Notch3 Mouse anti-Human, PE, Clone: MHN3-21, BD

Manufacturer: BD Biosciences

Select a Size

Pack Size SKU Availability Price
Each of 1 BDB563593-Each-of-1 In Stock ₹ 25,409.50

BDB563593 - Each of 1

₹ 25,409.50

In Stock

Quantity

1

Base Price: ₹ 25,409.50

GST (18%): ₹ 4,573.71

Total Price: ₹ 29,983.21

Antigen

Notch3

Classification

Monoclonal

Conjugate

PE

Formulation

Aqueous buffered solution containing BSA and ≤0.09% sodium azide.

Immunogen

Human Notch3 Recombinant Protein

Quantity

50 Tests

Primary or Secondary

Primary

Content And Storage

Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.

Applications

Flow Cytometry

Clone

MHN3-21

Description

NOTC3; CADASIL; CASIL

Host Species

Mouse

Purification Method

Affinity Purified

Regulatory Status

RUO

Target Species

Human

Isotype

IgG1 κ

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Description

  • Description The MHN3-21 monoclonal antibody specifically binds to an extracellular domain of human Notch3
  • Notch3 is a type 1 transmembrane glycoprotein receptor and member of the Notch family that includes Notch1-Notch4
  • The Notch3 precursor is cleaved in the Golgi and presents as a cell surface heterodimeric receptor
  • The Notch3 receptor can bind to several membrane-bound ligands including Jagged1, Jagged2 and Delta1
  • Upon ligand binding, Notch3 undergoes proteolytic cleavage that results in the release of the Notch intracellular domain, NICD
  • NICD translocates to the nucleus where it can form a transcriptional activator complex with various transcription factors
  • These multimeric complexes either positively or negatively regulate the expression of multiple genes including those that orchestrate many facets of embryonic development and the subsequent functioning of organ systems such as the hematopoietic, immune, nervous and cardiovascular systems
  • Notch3 is reportedly expressed by monocytes but not by CD34+ cells and most types of normal lymphocytes
  • Notch3 has also been implicated in the development of T cell neoplasia
  • Notch3 is expressed in vascular smooth muscle cells and plays a key role in neural development
  • Mutations in Notch3 have been identified as the underlying cause of CADASIL, a cerebral autosomal dominant disease that is the most common form of hereditary stroke disorder.