Research of Hurler-scheie Syndrome has been linked to Mucopolysaccharidosis I, Mucopolysaccharidoses, Pfaundler-hurler Syndrome, Mucopolysaccharidosis V, Lysosomal Storage Diseases. The study of Hurler-scheie Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hurler-scheie Syndrome include Tooth Eruption, Synaptic Transmission, Rna Processing, Excretion. These pathways complement our catalog of research reagents for the study of Hurler-scheie Syndrome including antibodies and ELISA kits against ALPHA-L-IDURONIDASE, CAT, CRAT, ERG, IDUA.
Top Research Reagents
We have 541 products for the study of Hurler-scheie Syndrome that can be applied to Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Immunohistochemistry-Paraffin: Glutaminyl-peptide Cyclotransferase/QPCT Antibody [NBP1-81838] - Staining in human adrenal gland and liver tissues using anti-QPCT antibody. Corresponding QPCT RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/Glutaminyl-peptide-Cyclotransferase-QPCT-Antibody-Immunohistochemistry-Paraffin-NBP1-81838-img0010.jpg)
![Western Blot: Glutaminyl-peptide Cyclotransferase/QPCT Antibody [NBP1-81838] - Analysis in human cell line SK-MEL-30.](https://images.novusbio.com/fullsize/Glutaminyl-peptide-Cyclotransferase-QPCT-Antibody-Western-Blot-NBP1-81838-img0006.jpg)
![Immunohistochemistry-Paraffin: CRAT Antibody [NBP1-86616] - Analysis in human testis and lymph node tissues. Corresponding CRAT RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/CRAT-Antibody-Immunohistochemistry-Paraffin-NBP1-86616-img0014.jpg)
![Western Blot: CRAT Antibody [NBP1-86616] - Analysis using Anti-CRAT antibody NBP1-86616 (A) shows similar pattern to independent antibody NBP1-86615 (B).](https://images.novusbio.com/fullsize/CRAT-Antibody-Western-Blot-NBP1-86616-img0011.jpg)
![Western Blot: GLYAT Antibody [NBP2-58917] - Western blot analysis in human cell line RT-4, human cell line U-251 MG, human plasma and human liver tissue.](https://images.novusbio.com/fullsize/GLYAT-Antibody-Western-Blot-NBP2-58917-img0002.jpg)
![Immunohistochemistry-Paraffin: GLYAT Antibody [NBP2-58917] - Staining of human skeletal muscle.](https://images.novusbio.com/fullsize/GLYAT-Antibody-Immunohistochemistry-Paraffin-NBP2-58917-img0010.jpg)
![Western Blot: ERG Antibody [NBP2-60655] - Total protein from Human THP-1, Jurkat and K562 cells was separated on a 7.5% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 2.0 ug/ml anti-ERG in blocking buffer and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.](https://images.novusbio.com/fullsize/ERG-Antibody-Western-Blot-NBP2-60655-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: ERG Antibody [NBP2-60655] - HeLa cells were fixed for 10 minutes using 10% formalin and then permeabilized for 5 minutes using 1X TBS + 0.5% Triton-X100. The cells were incubated with anti-ERG at 5 ug/ml overnight at 4C and detected with an anti-rabbit Dylight 488 (Green) at a 1:500 dilution. Alpha tubulin (DM1A) NB100-690 was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse Dylight 550 (Red) at a 1:500 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 40X objective.](https://images.novusbio.com/fullsize/ERG-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-60655-img0001.jpg)
![Western Blot: Kv11.1 Antibody [NBP3-03109] - Analysis of extracts of various cell lines, using Kv11.1 antibody at 1:500 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhan](https://images.novusbio.com/fullsize/Kv11.1-Antibody-Western-Blot-NBP3-03109-img0004.jpg)
![Immunohistochemistry-Paraffin: Kv11.1 Antibody [NBP3-03109] - Human lung cancer using KCNH2 antibody at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](https://images.novusbio.com/fullsize/Kv11.1-Antibody-Immunohistochemistry-Paraffin-NBP3-03109-img0003.jpg)
