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NAP1L3 (P-14) Antikörper: sc-131618

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  • goat polyclonal IgG, 200 µg/ml
  • epitope mapping near the C-terminus of NAP1L3 of human origin
  • recommended for detection of NAP1L3 of mouse, rat and human origin by WB, IF and ELISA; non cross-reactive with other NALP1L family members
  • blocking peptide, sc-131618 P
 
Weitere NAP1L Antikörper ...
 
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Empfohlene Supportprodukte:
(Klicken Sie auf die gewünschte Anwendung um passenden Supportprodukte anzuzeigen.)
WB   IF   siRNA  
 
Spezies Gen Gen ID Chromosomaler Locus mRNA (Isoform) Accession # Protein Accession # OMIM™ Nummer
Human NAP1L3 4675 Xq21.32 Q99457
300117
Maus Nap1l3 54561 X E3 Q794H2
n.n.
 
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 Bestellinformationen
ProduktKatalog #MengePreisAnzahlKaufFavorit
NAP1L3 (P-14) sc-131618 200 µg/ml $279
NAP1L3 (P-14) P sc-131618 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gen Silencer (Klicken Sie auf den Produktnamen für weitere Informationen.)
ProduktKatalog #MengePreisAnzahlKaufFavorit
NAP1L3 siRNA (h) sc-91058 10 µM $258
NAP1L3 siRNA (m) sc-149825 10 µM $258
NAP1L3 (h)-PR sc-91058-PR 10 µM $23
NAP1L3 (m)-PR sc-149825-PR 10 µM $23
 shRNA Plasmide (Klicken Sie auf den Produktnamen für weitere Informationen.)
ProduktKatalog #MengePreisAnzahlKaufFavorit
NAP1L3 shRNA Plasmid (h) sc-91058-SH 20 µg $520
NAP1L3 shRNA Plasmid (m) sc-149825-SH 20 µg $520
 shRNA Lentivirale Partikel (Klicken Sie auf den Produktnamen für weitere Informationen.)
ProduktKatalog #MengePreisAnzahlKaufFavorit
NAP1L3 shRNA (h) Lentiviral Particles sc-91058-V 200 µl $625
NAP1L3 shRNA (m) Lentiviral Particles sc-149825-V 200 µl $625

NAP1L3 Background Information
Proper nucleosome assembly is critical for compacting DNA into chromatin. NAP1 (nucleosome assembly protein 1) is a nuclear protein that acts as a transcriptional regulator and functions in nucleosome assembly. NAP1L3 (nucleosome assembly protein 1-like 3), also known as MB20 or NPL3, is a 506 amino acid nuclear protein belonging to the nucleosome assembly protein (NAP) family. Expressed in human brain with weak expression in heart, NAP1L3 is encoded by a gene mapping to human chromosome Xq21.32, which is in close proximity to a region closely linked to several X-linked mental retardation syndromes. Containing nearly 153 million base pairs and housing over 1,000 genes, chromosome X acts in conjunction with chromosome Y to determine sex. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.