santa cruz biotechnology, inc.
SCBT Logo

Benvenuto!       Visualizza carrello     Quick Order

AADACL1 (T-14) Anticorpo: sc-99749

 |  Scheda tecnica
  • goat polyclonal IgG, 200 µg/ml
  • epitope mapping within an internal region of AADACL1 of human origin
  • recommended for detection of AADACL1 of mouse, rat and human origin by WB, IF and ELISA; also reactive with additional species, including equine, canine, bovine, porcine and avian
  • blocking peptide, sc-99749 P
 
Altri AADAC Anticorpi ...
 
Informazioni ordini
Recommended Support Products:
(click button of application of choice)
WB   IF  
 
Specie Nome del gene Codice del gene Locus cromosoma Isoform (mRNA) Accession # codice accesso proteina Numero d'ordine
Umano NCEH1 57552 3q26.31 NM_001146276, NM_001146277, NM_001146278, NM_020792 Q6PIU2
n/a
Mouse Nceh1 320024 3 A3 NM_178772 Q8BLF1
N/A
 
Seleziona la valuta

 Informazioni ordini
Nome del prodottoCodice del prodottoUnitàPrezzoQuantitàAggiungiFavorites
AADACL1 (T-14) sc-99749 200 µg/ml $279
AADACL1 (T-14) P sc-99749 P
(peptide)
100 µg/0.5 ml $61

AADACL1 Background Information
The assembly of very-low-density lipoproteins (VLDLs) in the secretory apparatus of the hepatocyte relies on the mobilization of triacylglycerol (TAG) from the cytosolic pool by lipolysis and re-esterification. However, some of the re-esterified TAG products are returned to the cytosolic pool in the liver, which protects vulnerable body tissues from excess lipotoxic non-esterified fatty acids in the plasma. Some of the lipases involved in this process include arylacetamide deacetylase (AADAC) and its related proteins AADACL1 and AADACL2. AADAC, a single pass type II membrane protein of the endoplasmic reticulum, is expressed in hepatocytes, intestinal mucosal cells, pancreas and adrenal gland. It plays an important role in the metabolic activation of arylamine substrates to ultimate carcinogens. AADACL1 hydrolyzes the metabolic intermediate 2-acetyl monoalkylglycerol, and its inactivation results in disruption of ether lipid metabolism in cancer cells and impaired cell migration and tumor growth.