Neurogenic Locus Notch Homolog Protein 1 (Notch1) Antibody (ATTO390)

Este producto es parte de NOTCH - Neurogenic locus notch homolog protein
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650€ (100 µg)

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935106861
info@markelab.com
name
Neurogenic Locus Notch Homolog Protein 1 (Notch1) Antibody (ATTO390)
category
Primary Antibodies
provider
Abbexa
reference
abx440190
tested applications
WB, IF/ICC

Description

Notch1 Antibody is a Mouse Monoclonal against Notch1.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Neurogenic Locus Notch Homolog Protein 1 (Notch1)
Host
Mouse
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Monoclonal
Conjugation
ATTO390
Isotype
IgG1
Purification
Purified by Protein G.
Size 1
100 µg
Tested Applications
WB, IF/ICC
Buffer
PBS, pH 7.4, 50% glycerol, 0.09% sodium azide.
Availability
Shipped within 5-12 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q01705
Gene ID
18128
NCBI Accession
NP_032740.3
Alias
AOS5,AOVD1,TAN1,Hn1,Translocation-associated notch protein TAN-1,notch receptor 1
Background
Antibody anti-NOTCH1
Status
RUO
Note
Concentration: 1 mg/ml - 

Descripción

NOTCH1 is a transmembrane receptor of the Notch signaling pathway, which regulates critical processes such as cell fate determination, proliferation, differentiation, and apoptosis during development and tissue homeostasis. Upon ligand binding (e.g., Jagged or Delta-like ligands), the NOTCH1 receptor undergoes proteolytic cleavage, releasing its intracellular domain (NICD). NICD translocates to the nucleus, activating transcription of target genes, including HES and HEY family members, to modulate cell behavior. Dysregulation of NOTCH1 contributes to various diseases, including cancers such as T-cell acute lymphoblastic leukemia (T-ALL), where activating mutations drive aberrant proliferation. In addition, NOTCH1 plays a role in cardiovascular development, neural differentiation, and immune system regulation. Knockout studies reveal embryonic lethality due to disrupted vascular development and neurogenesis, demonstrating its essential role in embryonic and adult tissue homeostasis, cellular differentiation, and oncogenesis.

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This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and head and neck squamous cell carcinoma.

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