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UBAC2 (N-15) Anticorps: sc-84647

 |  Fiche technique
  • rabbit polyclonal IgG, 100µg/ml
  • epitope mapping near the C-terminus of UBAC2 of human origin
  • recommended for detection of UBAC2 of mouse and human origin by WB, IF and ELISA; non cross-reactive with isoforms 2, 3, and 4; also reactive with additional species, including equine and bovine
  • blocking peptide, sc-84647 P
 
D'autres UBAC Anticorps ...
 
Conditions Générales
Accessoires recommandés:
(Cliquez sur l'application voulue)
 
Espèce Nom du Gène Gene ID Localisation chromosomique Numéro d'accession de l'isoforme (ARNm) Numéro d'accession de la protéine Numéro OMIM™
Humain UBAC2 337867 13q32.3 Q8NBM4
n/a
 
Monnaie

 Conditions Générales
Nom du produitRéférenceCond.Prix HTQuantitéAcheterFavoris
UBAC2 (N-15) sc-84647 100 µg/ml $279
UBAC2 (N-15) P sc-84647 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gene Silencers (Cliquez sur le nom du produit pour plus d'informations)
Nom du produitRéférenceCond.Prix HTQuantitéAcheterFavoris
UBAC2 siRNA (h) sc-76785 10 µM $258
UBAC2 siRNA (m) sc-154841 10 µM $258
UBAC2 (h)-PR sc-76785-PR 10 µM $23
UBAC2 (m)-PR sc-154841-PR 10 µM $23
 shARN Plasmides (Cliquez sur le nom du produit pour plus d'informations)
Nom du produitRéférenceCond.Prix HTQuantitéAcheterFavoris
UBAC2 shRNA Plasmid (h) sc-76785-SH 20 µg $520
UBAC2 shRNA Plasmid (m) sc-154841-SH 20 µg $520
 shARN Particules Lentivirales (Cliquez sur le nom du produit pour plus d'informations)
Nom du produitRéférenceCond.Prix HTQuantitéAcheterFavoris
UBAC2 shRNA (h) Lentiviral Particles sc-76785-V 200 µl $625
UBAC2 shRNA (m) Lentiviral Particles sc-154841-V 200 µl $625

UBAC2 Background Information
UBAC2 (ubiquitin-associated domain-containing protein 2), also known as PHGDHL1 (phosphoglycerate dehydrogenase-like protein 1), is a 344 amino acid multi-pass membrane protein that contains one UBA domain and is expressed as multiple alternatively spliced isoforms. The gene encoding UBAC2 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4% of the human genome. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.