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Anti-Notch 1 Antibody

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产品名称: Anti-Notch 1 Antibody
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Anti-Notch 1 Antibody


Anti-Notch 1 Antibody  的详细介绍
Name: Anti-Notch 1 Antibody
See all Notch1 primary antibodies
Description: Rabbit monoclonal antibody to Notch 1.
Applications: WB, IHC, IF, IP, FC
Dilutions: WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, ICC: 1:50 - 1:200, IF: 1:50 - 1:100, IP: 1:20 - 1:50, FC: 1:20 - 1:50.
Reactivity: Human, Mouse
Immunogen: Recombinant protein of human NOTCH1.
Host: Rabbit
Clonality: Monoclonal
Isotype: IgG
Conjugate: Unconjugated
Purification: Affinity purification.
Product Form: Liquid
Formulation: Supplied in Phosphate Buffered Saline, pH 7.30, with 0.02% Sodium Azide and 50% Glycerol.
Storage: Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Function: Functions as a receptor for membrane-bound ligands Jagged1, Jagged2 and Delta1 to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs. Involved in angiogenesis; negatively regulates endothelial cell proliferation and migration and angiogenic sprouting. Involved in the maturation of both CD4+ and CD8+ cells in the thymus. Important for follicular differentiation and possibly cell fate selection within the follicle. During cerebellar development, functions as a receptor for neuronal DNER and is involved in the differentiation of Bergmann glia. Represses neuronal and myogenic differentiation. May play an essential role in postimplantation development, probably in some aspect of cell specification and/or differentiation. May be involved in mesoderm development, somite formation and neurogenesis. May enhance HIF1A function by sequestering HIF1AN away from HIF1A. Required for the THBS4 function in regulating protective astrogenesis from the subventricular zone (SVZ) niche after injury. Involved in determination of left/right symmetry by modulating the balance between motile and immotile (sensory) cilia at the left-right organiser (LRO).
Tissue Specificity: In fetal tissues most abundant in spleen, brain stem and lung. Also present in most ***** tissues where it is found mainly in lymphoid tissues.
Involvement in Disease: Aortic valve disease 1: A common defect in the aortic valve in which two rather than three leaflets are present. It is often associated with aortic valve calcification, stenosis and insufficiency. In extreme cases, the blood flow may be so restricted that the left ventricle fails to grow, resulting in hypoplastic left heart syndrome.

Adams-Oliver syndrome 5: A form of Adams-Oliver syndrome, a disorder characterized by the congenital absence of skin (aplasia cutis congenita) in combination with transverse limb defects. Aplasia cutis congenita can be located anywhere on the body, but in the vast majority of the cases, it is present on the posterior parietal region where it is often associated with an underlying defect of the parietal bones. Limb abnormalities are typically limb truncation defects affecting the distal phalanges or entire digits (true ectrodactyly). Only rarely, metatarsals/metacarpals or more proximal limb structures are also affected. Apart from transverse limb defects, syndactyly, most commonly of second and third toes, can also be observed. The clinical features are highly variable and can also include cardiovascular malformations, brain abnormalities and vascular defects such as cutis marmorata and dilated scalp veins.
Sequence Similarities: Belongs to the NOTCH family.
Post-Translational Modification: Synthesized in the endoplasmic reticulum as an inactive form which is proteolytically cleaved by a furin-like convertase in the trans-Golgi network before it reaches the plasma membrane to yield an active, ligand-accessible form. Cleavage results in a C-terminal fragment N(TM) and a N-terminal fragment N(EC). Following ligand binding, it is cleaved by ADAM17 to yield a membrane-associated intermediate fragment called notch extracellular truncation (NEXT). Following endocytosis, this fragment is then cleaved by presenilin dependent gamma-secretase to release a notch-derived peptide containing the intracellular domain (NICD) from the membrane.
Cellular Location: Cell membrane.
Database Links:
  • Entrez Gene: 4851?Human
  • Entrez Gene: 18128?Mouse
  • Omim: 190198?Human
  • SwissProt: P46531?Human
  • SwissProt: Q01705?Mouse
  • Unigene: 495473?Human
  • Unigene: 290610?Mouse
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    Synonyms:
  • 9930111A19Rik Antibody
  • AOS5 Antibody
  • AOVD1 Antibody
  • hN1 Antibody
  • Lin-12 Antibody
  • LIN12 Antibody
  • Mis6 Antibody
  • Motch A Antibody
  • mT14 Antibody
  • Neurogenic locus notch homolog protein 1 Antibody
  • Neurogenic locus notch protein homolog Antibody
  • NICD Antibody
  • NOTC1_HUMAN Antibody
  • NOTCH Antibody
  • Notch 1 Antibody
  • Notch 1 intracellular domain Antibody
  • Notch gene homolog 1 (Drosophila) Antibody
  • Notch homolog 1, translocation-associated (Drosophila) Antibody
  • NOTCH, Drosophila, homolog of, 1 Antibody
  • Notch1 Antibody
  • TAN1 Antibody
  • Translocation associated notch homolog Antibody
  • Translocation associated notch protein TAN 1 Antibody
  • Translocation-associated notch protein TAN-1 Antibody
  • xotch Antibody
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    Information: Target information shown above is from the UniProt Consortium.
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