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HAGHL (L-12) Anticuerpo: sc-136705

 |  Panfleto informativo:
  • goat polyclonal IgG, 200 µg/ml
  • epitope mapping near the C-terminus of HAGHL of human origin
  • recommended for detection of HAGHL of human origin by WB, IF and ELISA
  • blocking peptide, sc-136705 P
 
Adicional HAGHL Isotipos del anticuerpo ...
 
Información sobre pedidos
Productos Recomendados para Ayudar:
(Haga clic en el botón para el applicación de su selección)
WB   IF   ARNic  
 
Especie Nombre del Gen Identificacion del Gen Ubicacion del cromosoma Numero de Accesion de Isoforma (ARNm) Numero de Accesion de la Proteina Número de pedido:
Humano HAGHL 84264 16p13.3 Q6PII5
n/a
Humano HAGHL 84264 16p13.3 NM_032304, NM_207112 NP_115680
n/a
 
Indique la moneda

 Información sobre pedidos
Descripción del productoNúmero de catálogoUnidadPrecioCantidadSumarFavorites
HAGHL (L-12) sc-136705 200 µg/ml $279
HAGHL (L-12) P sc-136705 P
(peptide)
100 µg/0.5 ml $61
 Silenciadores de Genes siRNA (click product name for more information)
Descripción del productoNúmero de catálogoUnidadPrecioCantidadSumarFavorites
HAGHL siRNA (h) sc-93220 10 µM $258
HAGHL (h)-PR sc-93220-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Descripción del productoNúmero de catálogoUnidadPrecioCantidadSumarFavorites
HAGHL shRNA Plasmid (h) sc-93220-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Descripción del productoNúmero de catálogoUnidadPrecioCantidadSumarFavorites
HAGHL shRNA (h) Lentiviral Particles sc-93220-V 200 µl $625

HAGHL Background Information
The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.