Western Blot: Tissue alpha-L-Fucosidase/FUCA1 Antibody (1D4) [H00002517-M01] - Analysis of FUCA1 expression in transfected 293T cell line by FUCA1 monoclonal antibody (M01), clone 1D4. Lane 1: FUCA1 transfected ...read more
Western Blot: Tissue alpha-L-Fucosidase/FUCA1 Antibody (1D4) [H00002517-M01] - FUCA1 monoclonal antibody (M01), clone 1D4 Western Blot analysis of FUCA1 expression in K-562 ( Cat # L009V1 ).
Tissue alpha-L-Fucosidase/FUCA1 Antibody (1D4) - Azide and BSA Free Summary
Description
Quality control test: Antibody Reactive Against Recombinant Protein.
Immunogen
FUCA1 (AAH17338, 23 a.a. ~ 461 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. VRRAQPPRRYTPDWPSLDSRPLPAWFDEAKFGVFIHWGVFSVPAWGSEWFWWHWQGEGRPQYQRFMRDNYPPGFSYADFGPQFTARFFHPEEWADLFQAAGAKYVVLTTKHHEGFTNWPSPVSWNWNSKDVGPHRDLVGELGTALRKRNIRYGLYHSLLEWFHPLYLLDKKNGFKTQHFVSAKTMPELYDLVNSYKPDLIWSDGEWECPDTYWNSTNFLSWLYNDSPVKDEVVVNDRWGQNCSCHHGGYYNCEDKFKPQSLPDHKWEMCTSIDKFSWGYRRDMALSDVTEESEIISELVQTVSLGGNYLLNIGPTKDGLIVPIFQERLLAVGKWLSINGEAIYASKPWRVQWEKNTTSVWYTSKGSAVYAIFLHWPENGVLNLESPITTSTTKITMLGIQGDLKWSTDPDKGLFISLPQLPPSAVPAEFAWTIKLTGVK
Specificity
FUCA1 - fucosidase, alpha-L- 1, tissue
Isotype
IgG2b Kappa
Clonality
Monoclonal
Host
Mouse
Gene
FUCA1
Purity
IgG purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.
Antibody reactivity against cell lysate and recombinant protein for WB. It has also been used for ELISA. Use in Immunohistochemistry reported in scientific literature (PMID: 26204487).
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Buffer
In 1x PBS, pH 7.4
Preservative
No Preservative
Purity
IgG purified
Notes
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for Tissue alpha-L-Fucosidase/FUCA1 Antibody (1D4) - Azide and BSA Free
Alpha-L-fucosidase 1
Alpha-L-fucosidase I
Alpha-L-fucoside fucohydrolase 1
EC 3.2.1
EC 3.2.1.51
FUCA
FUCA1
fucosidase, alpha-L- 1, tissue
Tissue alphaLFucosidase
Tissue alpha-L-Fucosidase
Background
Fucosidosis is an autosomal recessive lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues. Different phenotypes include clinical features such as neurologic deterioration, growth retardation, visceromegaly, and seizures in a severe early form; coarse facial features, angiokeratoma corporis diffusum, spasticity and delayed psychomotor development in a longer surviving form; and an unusual spondylometaphyseoepiphyseal dysplasia in yet another form.[supplied by OMIM]
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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