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CUTC Antibody (S-16): sc-160262

 |  Datasheet

(Based on data analysis)

  • CUTC Antibody (S-16) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping within an internal region of CUTC of human origin
  • recommended for detection of CUTC of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including equine, canine, bovine and porcine
  • blocking peptide, sc-160262 P
 

See additional CUTC Antibodies.

Ordering InformationGene Info
Recommended Support Products:
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WB   IP   IF   siRNA  
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
CUTC Antibody (S-16) sc-160262 200 µg/ml $279
CUTC (S-16) P sc-160262 P
(peptide)
 100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
CUTC siRNA (h) sc-90475 10 µM $258
CUTC siRNA (m) sc-142636 10 µM $258
CUTC (h)-PR sc-90475-PR 10 µM, 20 µl $23
CUTC (m)-PR sc-142636-PR 10 µM, 20 µl $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
CUTC shRNA Plasmid (h) sc-90475-SH 20 µg $520
CUTC shRNA Plasmid (m) sc-142636-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
CUTC shRNA (h) Lentiviral Particles sc-90475-V 200 µl $625
CUTC shRNA (m) Lentiviral Particles sc-142636-V 200 µl $625
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human CUTC 51076 10q24.2 Q9NTM9
 610101
Mouse Cutc 66388 19 C3 Q9D8X1
 N/A
 

Copper is an essential micronutrient used as a co-factor for several essential enzymes in all living organisms. Due to the high toxicity of copper, its metabolism is tightly regulated and defects in this regulation can cause Menkes (deficiency) or Wilson (accumulation) disease in various tissue. CUTC (cutC copper transporter homolog (E. coli)), also known as CGI-32, is a 273 amino acid protein belonging to the cutC family. CUTC is involved in copper homeostasis and is encoded by a gene located on human chromosome 10, which contains over 800 genes and 135 million nucleotides. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. Other chromosome 10 associated disorders include Cockayne syndrome, tetrahydrobiopterin deficiency and trisomy 10.

CUTC Antibody (S-16) Data
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sc-160262
CUTC (S-16): sc-160262. Western blot analysis of CUTC expression in Colo 320 DM (A), Jurkat (B) and HeLa (C) whole cell lysates.
sc-160262
CUTC (S-16): sc-160262. Western blot analysis of CUTC expression in non-transfected: sc-117752 (A) and mouse CUTC transfected: sc-119529 (B) 293T whole cell lysates.
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