The Notch1 Monoclonal Antibody (CAB19090) is a high-quality antibody developed for reliable detection and analysis of target proteins. This antibody, produced using cutting-edge technology, offers high specificity and sensitivity in detecting NOTCH1 protein levels in human samples, making it ideal for Western blotting and immunohistochemistry applications.NOTCH1 is a critical regulator of cell fate decisions and plays a crucial role in numerous biological processes, including embryonic development, tissue homeostasis, and immune response modulation.
This antibody is validated for use in WB, IP, ELISA applications and has demonstrated reactivity against Human, Mouse samples.
Product Name:
Notch1 Monoclonal Antibody
SKU:
CAB19090
Size:
20μL, 100μL
Reactivity:
Human, Mouse
Clone Number:
ARC0285
Conjugate:
Unconjugated
Immunogen:
Synthetic peptide. This information is considered to be commercially sensitive.
0.5μg-4μg antibody for 200μg-400μg extracts of whole cells
ELISA
Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Synonyms:
hN1, AOS5, TAN1, AOVD1, Notch1
Positive Sample:
Jurkat, Mouse lung
Cellular Localization:
Cell Membrane, Nucleus, Single-Pass Type I Membrane Protein.
Calculated MW:
273kDa
Observed MW:
120kDa/300kDa
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.
Purification Method
Affinity purification
Gene ID
4851
RRID
AB_2862582
Buffer Information
Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS containing 50% glycerol and 0.05% BSA, preserved with proclin300 or sodium azide, pH 7.3.
Western blot analysis of various lysates using Notch1 Rabbit mAb (CAB19090) at 1:1000 dilution incubated overnight at 4℃. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25 μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (AbGn00020). Exposure time: 90s.
Immunoprecipitation analysis of 200 μg extracts of 293T cells using 3 μg Notch1 antibody (CAB19090). Western blot was performed from the immunoprecipitate using Notch1 antibody (CAB19090) at a dilution of 1:1000.
