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Recombinant Rabbit Anti-NOTCH3 Monoclonal Antibody
Recombinant Rabbit Anti-NOTCH3 Monoclonal Antibody
CADASIL; CADASIL1; CARASIL1; CASIL; FPLD1; IMF2; LMNS; N3; hpbk; NOTC3_HUMAN; NOTCH3; Notch 3; NOTC3_MOUSE; NOTC3_RAT; notch receptor 3; Notch (Drosophila) homolog 3; Notch homolog 3 (Drosophila); NOTCH3 (Cleaved-Asp1628); Neurogenic locus notch homolog p
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  • NO.:SLA3561M
    React Species:Human, Rat
    Immunogen Species:Rabbit
    Clonality:Recombinant
    Applications:WB, IHC-P, IHC-F, IF, ELISA, IP
    Gene name:NOTCH3
    UniProt Entry:Q9UM47
    NCBI Gene Entry:4854
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Product NameRecombinant Rabbit Anti-NOTCH3 Monoclonal Antibody
Cat No.SLA3561M
AliasCADASIL; CADASIL1; CARASIL1; CASIL; FPLD1; IMF2; LMNS; N3; hpbk; NOTC3_HUMAN; NOTCH3; Notch 3; NOTC3_MOUSE; NOTC3_RAT; notch receptor 3; Notch (Drosophila) homolog 3; Notch homolog 3 (Drosophila); NOTCH3 (Cleaved-Asp1628); Neurogenic locus notch homolog protein 3; [Cleaved into: Notch 3 extracellular truncation; Notch 3 intracellular domain]
Host SpeciesRabbit
IsotypeIgG
ClonalityMonoclonal
Clone No.11A9
React SpeciesHuman,Rat
ApplicationsWB (1:500-2000)
IHC-P (1:50-200)
IHC-F (1:50-200)
IF (1:50-200)
ELISA (1:5000-10000)
IP (1:50-200)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
Purificationaffinity purified by Protein A
Gene ID4854
Swiss-ProtQ9UM47
Storage0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
BackgroundThis gene encodes the third discovered human homologue of the Drosophilia melanogaster type I membrane protein notch. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signalling pathway that plays a key role in neural development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remains to be determined. Mutations in NOTCH3 have been identified as the underlying cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). [provided by RefSeq, Jul 2008]
AttentionThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.

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