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LRWD1 Antibody (S-12): sc-136741

 |  Datasheet

(Based on data analysis)

  • LRWD1 Antibody (S-12) is a rabbit polyclonal IgG provided at 100 µg/ml
  • epitope mapping within an internal region of LRWD1 of human origin
  • recommended for detection of LRWD1 of mouse, rat and human origin by WB, IP, IF and ELISA
  • blocking peptide, sc-136741 P
 

See additional LRWD Antibodies including LRWD and LRWD1.

Ordering InformationGene Info
Recommended Support Products:
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WB   IP   IF   siRNA  
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 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
LRWD1 Antibody (S-12) sc-136741 100 µg/ml $279
LRWD1 (S-12) sc-136741 P
(peptide)
 100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
LRWD1 siRNA (h) sc-89721 10 µM $258
LRWD1 siRNA (m) sc-149127 10 µM $258
LRWD1 (h)-PR sc-89721-PR 10 µM, 20 µl $23
LRWD1 (m)-PR sc-149127-PR 10 µM, 20 µl $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
LRWD1 shRNA Plasmid (h) sc-89721-SH 20 µg $520
LRWD1 shRNA Plasmid (m) sc-149127-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
LRWD1 shRNA (h) Lentiviral Particles sc-89721-V 200 µl $625
LRWD1 shRNA (m) Lentiviral Particles sc-149127-V 200 µl $625
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human LRWD1 222229 7q22.1 Q9UFC0
 n/a
Mouse Lrwd1 71735 5 G2 Q8BUI3
 N/A
 

LRWD1 (leucine-rich repeats and WD repeat domain containing 1) is a 647 amino acid protein that contains five WD domains and three LRR (leucine-rich) repeats. LRWD1 undergoes post-translational phosphorylation, most likely by ATR or ATM, and is encoded by a gene that maps to human chromosome 7. 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.

LRWD1 Antibody (S-12) Data
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sc-136741
LRWD1 (S-12): sc-136741. Western blot analysis of LRWD1 expression in LADMAC (A) and WI 38 (B) whole cell lysates and mouse thymus (C) tissue extract .
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