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IFI-44L (G-20) Antibody: sc-101981

 |  Datasheet
  • rabbit polyclonal IgG, 100µg/ml
  • raised against IFI-44L of human origin
  • recommended for detection of IFI-44L of human origin by WB, IP, IF, IHC(P) and ELISA
 
Additional IFI Antibodies ...
 
Ordering InformationProduct Citations
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 IFI44L 10964 1p31.1 NM_006820 NP_006811
n/a
 
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 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
IFI-44L (G-20) sc-101981 100 µg/ml $279
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
IFI-44L siRNA (h) sc-78896 10 µM $258
IFI-44L (h)-PR sc-78896-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
IFI-44L shRNA Plasmid (h) sc-78896-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
IFI-44L shRNA (h) Lentiviral Particles sc-78896-V 200 µl $625
 WB Positive Control Cell Lysates (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
Jurkat Whole Cell Lysate sc-2204 500 µg/200 µl $104
Jurkat nuclear extract sc-2132 1000 µg $143

IFI-44L Background Information
Interferon-induced protein 44-like (IFI-44L), also known as C1orf29, is a 452 amino acid cytoplasmic protein that shares some sequence similarities with IFI-44. IFI-44 is a cytoplasmic protein that aggregates to form microtubule structures. The genes that encode IFI-44L and IFI-44 are located on chromosome 1, which is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

IFI-44L (G-20) Product Citations
See how others have used IFI-44L (G-20): sc-101981 antibody and or IFI-44L (G-20) antibody conjugates.


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IFI-44L (G-20)
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IFI-44L (G-20): sc-101981. Immunoperoxidase staining of formalin fixed, paraffin-embedded human kidney tissue showing cytoplasmic and nuclear staining.
IFI-44L (G-20): sc-101981. Western blot analysis of IFI-44L expression in Jurkat whole cell lysate.
IFI-44L (G-20): sc-101981. Western blot analysis of IFI-44L expression in Jurkat nuclear extract.
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