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IFIT3 (E-22) Antibody: sc-133687

 |  Datasheet
  • rabbit polyclonal IgG, 50 µg/0.5 ml
  • recommended for detection of IFIT3 of human origin by WB, IP, IF, IHC(P) and ELISA
 
Additional IFIT Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IP   IF   IHC(P)   siRNA  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human IFIT3 3437 10q23.31 O14879
604650
 
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
IFIT3 (E-22) sc-133687 50 µg/0.5 ml $279
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
IFIT3 siRNA (h) sc-75326 10 µM $258
IFIT3 (h)-PR sc-75326-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
IFIT3 shRNA Plasmid (h) sc-75326-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
IFIT3 shRNA (h) Lentiviral Particles sc-75326-V 200 µl $625
 WB Positive Control Cell Lysates (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
HeLa Whole Cell Lysate sc-2200 500 µg/200 µl $104
Hep G2 Cell Lysate sc-2227 500 µg/200 µl $104

IFIT3 Background Information
The tetratricopeptide repeat (TPR) motif is a degenerate, 34 amino acid sequence found in many proteins and acts to mediate protein-protein interactions in various pathways. At the sequence level, there can be up to 16 tandem TPR repeats, each of which has a helix-turn-helix shape that stacks on other TPR repeats to achieve ligand binding specificity. IFIT3 (interferon-induced protein with tetratricopeptide repeats 3), also known as IRG2, IFI60, IFIT4, ISG60 or RIG-G, is a 490 amino acid protein that contains eight TPR repeats and may play a role in cell cycle regulation and cellular proliferation. The gene encoding IFIT3 maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

IFIT3 (E-22)
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IFIT3 (E-22): sc-133687. Western blot analysis of IFIT3 expression in HeLa whole cell lysate.
IFIT3 (E-22): sc-133687. Immunoperoxidase staining of formalin-fixed, paraffin-embedded human kidney tissue showing nuclear and cytoplasmic localization.
IFIT3 (E-22): sc-133687. Western blot analysis of IFIT3 expression in Hep G2 whole cell lysate.
IFIT3 (E-22): sc-133687. Western blot analysis of IFIT3 expression in Caki-1 (A) and COLO 320DM (B) whole cell lysates.
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