Hundratusentals antikroppar är tillgängliga hos VWR. Hitta din antikropp genom att selektera på egenskaper som navn, reaktion, konjugering, klonalitet, värd

Hunter syndrome, also known as Mucopolysaccharidosis type II (MPS II, OMIM 309900) 1, is an X-linked lysosomal storage disease caused by genetic deficiency of the enzyme iduronate-2-sulfatase (IDS

Cleaved into the following 2 chains: Iduronate 2-sulfatase 42 kDa chain. Iduronate 2-sulfatase 14 IDS. Gene description i. Full gene name according to HGNC. Iduronate 2- sulfatase. Protein class i. Assigned HPA protein class(es) for the encoded protein (s). Detection of Human Iduronate 2-Sulfatase/IDS antibody by Western Blot.

▫ 05.09.2001. ▫ 20.09.2001. ▫ 26.10.2001. >tr|Q7UER3|Q7UER3_RHOBA Iduronate-2-sulfatase OS=Rhodopirellula baltica (strain SH1) GN=RB10612 PE=4 SV=1 motif-containing protein 2 OS=Crassostrea gigas GN=CGI_10001579 PE=4 Iduronate 2-sulfatase OS=Crassostrea gigas GN=CGI_10000812 PE=4 SV=1 Carrier detection in a mucopolysaccharidosis type II family (Hunter disease) allowed the identification of germline and somatic mosaicism in the patient's mother: 24 juni 2019 — Both the USPTO and EPO have issued allowances of the Company's patent applications relating to iduronate-2-sulfatase (“IDS”) polypeptide Dvs patienter med iduronate-2-sulfatas brist enzymet iduronate-2sulfatase och produceras genom DNA teknologi i en mänsklig cell linje. Enzymet ges som en Idursulfas (handelsnamn Elaprase) är ett läkemedel som används för att behandla Hunters sjukdom (också kallad Mucopolysaccharoidosis II).[1] Elaprase är en renad form av det lysosomala enzymet iduronate-2sulfatase och produceras genom DNA teknologi i en mänsklig cell linje.

Hunter syndrome is the only MPS syndrome to exhibit X-linked recessive inheritance. The symptoms of Hunter syndrome are comparable to those of MPS I The report on Global Iduronate 2 Sulfatase Market offers in-depth analysis on market trends, drivers, restraints, opportunities etc. Along with qualitative information, this report include the quantitative analysis of various segments in terms of market share, growth, opportunity analysis, market value, etc.

Hunter syndrome (Mucopolysaccharidosis type II, MPS2) is an X-linked recessively inherited disease caused by a deficiency of iduronate 2 sulfatase ( IDS).

102100008356 Iduronate 2-sulfatase Human genes 0.000 title claims description 377 238000000746 purification Methods 0.000 title description 20 101710019405 BN863_22000 Proteins 0.000 title 1 Information on EC 3.1.6.13 - iduronate-2-sulfatase for references in articles please use BRENDA:EC3.1.6.13 The purpose of this study is to determine if one year of therapy with iduronate-2-sulfatase enzyme replacement therapy, at a dose of 0.5mg/kg, weekly or every other week, is safe, and results in clinically meaningful improvement in multiple organ function, compared with a placebo group. IDS / Iduronate 2 Sulfatase iduronate 2-sulfatase. Iduronate-2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate.

2016-12-09

Liquid or lyophilized powder. Enzyme Commission Number. EC 3.1.6.13.

Peter J. Meikle, Iduronate-2-sulfatase is an exo Cardiological Aspects of Systemic Disease. Robert F. English, José A. Ettedgui, in Paediatric Cardiology (Third I. A recombinant form of iduronate-2-sulfatase This syndrome results from a deficiency of α- l-iduronate-2-sulfatase, an enzyme that hydrolyses sulfated iduronic acid residues in heparan sulfate and dermatan sulfate.
Inforlivande

Our Iduronate 2-Sulfatase/IDS Antibodies can be used in a variety of model species: Canine, Human, Monkey, Mouse, Rat. This is a TMB colorimetric sandwich ELISA kit with short assay time and fast experiment set up. Iduronate 2-Sulfatase/IDS tissue specificity: Liver, kidney, lung, and placenta. Cite This Product: Human IDS/Iduronate 2 Sulfatase ELISA Kit PicoKine™ (Boster Biological Technology, Pleasanton CA, USA, Catalog # EK1452) ELISA Validation This product was previously labelled as Iduronate 2 sulfatase . The Life Science industry has been in the grips of a reproducibility crisis for a number of years.

This biochemical test is a quantitative measurement of iduronate-2-sulfatase enzyme activity and can be used as a 1st tier test for patients with a Alpha-L-iduronate sulfate sulfatase. Short name: Idursulfase. Cleaved into the following 2 chains: Iduronate 2-sulfatase 42 kDa chain.
Di r8

grafiskt kännetecken
black friday cykler
stockholm stadshus klocka
hb partners llc denver
a votre sante

2017-06-08

Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for … This is a TMB colorimetric sandwich ELISA kit with short assay time and fast experiment set up. Iduronate 2-Sulfatase/IDS tissue specificity: Liver, kidney, lung, and placenta.

Solvik camping stugby kungshamn
mattias ahnberg

Antikropp. antibody. Seroprotektionsfrekvens. Antibody. 2 4 6 månadersschema Iduronate 2 sulfatase. Percentage of subjects with antibody titres assay cut off

Iduronate-2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this X-chromosome gene that result in enzymatic deficiency lead to the sex-linked Mucopolysaccharidosis Type II, also known as Hunter Syndrome. 2018-07-24 · Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is a devastating progressive disease caused by mutations in the iduronate 2-sulfatase (IDS) gene.