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LANCL2 (Y-17) Anticorps: sc-79566

 |  Fiche technique
  • goat polyclonal IgG, 200µg/ml
  • epitope mapping within an internal region of LANCL2 of human origin
  • recommended for detection of LANCL2 of human origin by WB, IF and ELISA; also reactive with additional species, including equine, canine and bovine
  • blocking peptide, sc-79566 P
 
D'autres LANCL 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 LANCL2 55915 7p11.2 Q9NS86
n/a
 
Monnaie

 Conditions Générales
Nom du produitRéférenceCond.Prix HTQuantitéAcheterFavoris
LANCL2 (Y-17) sc-79566 200 µg/ml $279
LANCL2 (Y-17) P sc-79566 P
(peptide)
100 µg/0.5ml $61
 siRNA Gene Silencers (Cliquez sur le nom du produit pour plus d'informations)
Nom du produitRéférenceCond.Prix HTQuantitéAcheterFavoris
LANCL2 siRNA (h) sc-75407 10 µM $258
LANCL2 (h)-PR sc-75407-PR 10 µM $23
 shARN Plasmides (Cliquez sur le nom du produit pour plus d'informations)
Nom du produitRéférenceCond.Prix HTQuantitéAcheterFavoris
LANCL2 shRNA Plasmid (h) sc-75407-SH 20 µg $520
 shARN Particules Lentivirales (Cliquez sur le nom du produit pour plus d'informations)
Nom du produitRéférenceCond.Prix HTQuantitéAcheterFavoris
LANCL2 shRNA (h) Lentiviral Particles sc-75407-V 200 µl $625

LANCL2 Background Information
LANCL2 (LanC-like protein 2), also known as TASP (testis-specific adriamycin sensitivity protein) or GPR69B, is a 450 amino acid member of the LanC-like protein family. Localized to the nucleus, cytoplasm and cell membrane, LANCL2 is expressed highly in brain and testis. The gene that encodes LANCL2 maps to human chromosome 7 and is considered a bystander gene that is coamplified and overexpressed with EGFR in 20% of glioblastomas. Human Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.