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SEZ6L Antibody (D-19): sc-86856

 |  Datasheet

(Based on data analysis)
  • SEZ6L Antibody (D-19) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping within an extracellular domain of SEZ6L of human origin
  • recommended for detection of SEZ6L of human origin by WB, IF and ELISA; also reactive with additional species, including equine, canine and porcine
  • blocking peptide, sc-86856 P
 

See additional SEZ Antibodies including SEZ, SEZ6L2, SEZ6 and SEZ6L.

Ordering InformationGene Info
Recommended Support Products:
(click button of application of choice)
WB   IF   siRNA  
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 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
SEZ6L Antibody (D-19) sc-86856 200 µg/ml $279
SEZ6L (D-19) P sc-86856 P
(peptide)
 100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
SEZ6L siRNA (h) sc-76487 10 µM $258
SEZ6L (h)-PR sc-76487-PR 10 µM, 20 µl $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
SEZ6L shRNA Plasmid (h) sc-76487-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
SEZ6L shRNA (h) Lentiviral Particles sc-76487-V 200 µl $625
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human SEZ6L 23544 22q12.1 Q9BYH1
 607021
 

SEZ6L (seizure related 6 homolog-like) is a 1,024 amino acid single-pass type I membrane protein that localizes to the endoplasmic reticulum. Widely expressed, SEZ6L is a candidate tumor suppressor gene and may contribute to specialized endoplasmic reticulum functions in neurons. SEZ6L contains three CUB domains and five sushi (CCP/SCR) domains, which may be involved in protein-protein interactions and signal transduction. The gene encoding SEZ6L is located on human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.