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PHF13 Antibody (S-15): sc-103824

 |  Datasheet

(Based on data analysis)
  • PHF13 Antibody (S-15) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping within an internal region of PHF13 of human origin
  • recommended for detection of PHF13 of mouse, rat and human origin by WB, IF and ELISA; non cross-reactive with other PHF family members; also reactive with additional species, including equine, canine and bovine
  • blocking peptide, sc-103824 P
 

See additional PHF Antibodies including PHF, PHF1, PHF11, PHF14, PHF15, PHF23, PHF7, PHF2, PHF3, PHF5A, PHF6, PHF8, PHF10, PHF12, PHF13, PHF16, PHF19, PHF20, PHF21A, PHF21B and PHF20L1.

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

 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
PHF13 Antibody (S-15) sc-103824 200 µg/ml $279
PHF13 (S-15) P sc-103824 P
(peptide)
 100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
PHF13 siRNA (h) sc-78690 10 µM $258
PHF13 siRNA (m) sc-106406 10 µM $258
PHF13 (h)-PR sc-78690-PR 10 µM, 20 µl $23
PHF13 (m)-PR sc-106406-PR 10 µM, 20 µl $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
PHF13 shRNA Plasmid (h) sc-78690-SH 20 µg $520
PHF13 shRNA Plasmid (m) sc-106406-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
PHF13 shRNA (h) Lentiviral Particles sc-78690-V 200 µl $625
PHF13 shRNA (m) Lentiviral Particles sc-106406-V 200 µl $625
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human PHF13 148479 1p36.31 Q86YI8
 n/a
 

Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. PHF13 (PHD finger protein 13), also known as PHF5 or SPOC1, is a 300 amino acid protein that contains one PHD-type zinc finger, suggesting involvement in transcriptional regulation events. The gene encoding PHF13 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.