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Naglu N-Acetyl-Alpha-Glucosaminidase [ Homo Sapiens ]

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Product No. RPD161Hu01 Organism Species Homo sapiens (Human) Same name, Different species. All Human Mouse Rat Cavia Rabbit Simian Canine Porcine Bovine Caprine Multi Citation Dessen P NAGLU (N-acetyl-alpha-glucosaminidase) Atlas Genet Cytogenet Oncol Haematol. 2015-10-01

Phosphorylation of-N-acetylglucosaminidase secreted by human cells. (A ...

1. Homo sapiens N-acetyl-alpha-glucosaminidase (NAGLU), mRNA 2,475 bp linear mRNA NM_000263.4 GI:1519314272 Full genetic testing confirmed the diagnosis of Sanfilippo syndrome type B with a deficiency of alpha-N-acetylglucosaminidase caused by a homozygous mutation c.889C>T, p.

NAGLU基因的功能与作用机制解析

关于 Naglu 功能概要 Predicted to enable hydrolase activity. Predicted to act upstream of or within several processes, including cerebellar Purkinje cell layer development; locomotor rhythm; and

NAGLU – N-acetyl-alpha-glucosaminidase Synonym (s): NAG, Sanfilippo disease IIIB Previous symbol (s) and name (s): N-acetylglucosaminidase, alpha Type: gene with protein product A Novel Pathogenic Variant in NAGLU (N-Acetyl-Alpha-Glucosaminidase) gene Identified by Targeted Next-Generation Sequencing Followed by in Silico Analysis All UniProtKB/Swiss-Prot entries referenced in this entry, with possibility to download in different formats, align etc.

N-Acetylglucosaminidase also known as NAG β-NAG and NAG-5 plays an important role in the breakdown of glycoproteins by catalyzing the hydrolysis of

Recovery Matrices listed below were spiked with certain level of recombinant N-Acetyl Alpha-D-Glucosaminidase (NAGLU) and the recovery rates were calculated by comparing the

ポピュラーベクター Human 遺伝子 NAGLU

  • Human NAG/Alpha-N-acetylglucosaminidase ELISA Kit
  • Alpha-N-acetylglucosaminidase
  • ELISA Kit for N-Acetyl Alpha-D-Glucosaminidase

Although heparan sulphate has not been found in plants, the At5g13690 gene encoding the alpha- N -acetyl-glucosaminidase (NAGLU), an enzyme involved in its Recovery Matrices listed below were spiked with certain level of recombinant N-Acetyl Alpha-D-Glucosaminidase (NAGLU) ,etc. and the recovery rates were calculated by comparing the N-acetyl-alpha-glucosaminidase (Naglu) encodes a lysosomal enzyme that hydrolyzes terminal α-N-acetylglucosamine residues on the non-reducing end of the heparan

Recombinant Human NAGLU Protein, CF (Catalog # 7096-GH) degrades heparan sulfate by hydrolysis of terminal GlcNAc resides in N-acetyl-alpha-D

The high affinity binding of the HIRMAb-LL-NAGLU fusion protein to the HIR was retained. The NAGLU enzyme activity of this fusion protein was measured with a fluorometric enzyme assay UniProt is the world’s leading high-quality, comprehensive and freely accessible resource of protein sequence and functional information. La naglu (n-acetyl-alpha-glucosaminidase) es una enzima lisosomal que se encuentra en humanos y que juega un papel crucial en el proceso de hidrólisis de los glicanos

Die Dokumente dieser Website dienen nur der allgemeinen Information. Der Inhalt dieser Website ersetzt in keiner Weise eine professionelle Beratung oder Behandlung durch qualifizierte 本文将详细解析NAGLU基因的功能与作用机制,包括其在糖基水解酶家族中的角色、信号通路中的参与、以及与粘多糖贮积症III型的关系。 NAGLU基因的功能 NAGLU基因编码

重组Anti-NAGLU/NAG抗体 [EPR20708]

Matrices listed below were spiked with certain level of recombinant NAGLU and the recovery rates were calculated by comparing the measured value to the expected amount of NAGLU in

Human N-acetyl-alpha-glucosaminidase遺伝子をカスタムクローニングしたプラスミド、ウイルス、piggyBacベクターをベクタービルダーからお手頃価格で調達 Buy NAGLU, Recombinant, Human (Alpha-N-acetylglucosaminidase, N-acetyl-alpha-glucosaminidase, NAG, UFHSD, item number: N0017-06.20 from United States Biological at

Human NAG/Alpha-N-acetylglucosaminidase ELISA Kit The Human NAG (Alpha-N-Acetylglucosaminidase) ELISA Kit is a cutting-edge tool for the precise measurement of NAG Full genetic testing confirmed the diagnosis of Sanfilippo syndrome type B with a deficiency of Homo sapiens Human Same name alpha-N-acetylglucosaminidase caused by a homozygous mutation c.889C>T, p. Full genetic testing confirmed the diagnosis of Sanfilippo syndrome type B with a deficiency of alpha-N-acetylglucosaminidase caused by a homozygous mutation c.889C>T, p. (Arg297*) in

NAGLU – N-acetyl-alpha-glucosaminidase Sinónimo (s): NAG, Sanfilippo disease IIIB Símbolos e genes anteriore: N-acetylglucosaminidase, alpha Tipe: Gene com produto proteico localização α-N-アセチルグルコサミニダーゼ (Alpha-N-acetylglucosaminidase、 EC 3.2.1.50)は、 ムコ多糖症 の一種である サンフィリッポ症候群 と関連する 酵素 である。系統名は、 α-N-アセチル

Mucopolysaccharidosis III B (MPS III-B) is a rare lysosomal storage disorder caused by deficiencies in Alpha-N-acetylglucosaminidase (NAGLU) for which there is currently Canine Porcine Bovine Product No. MAD161Hu21 Organism Species Homo sapiens (Human) Same name, Different species. All Human Mouse Rat Cavia Rabbit Simian Canine Porcine Bovine Caprine Multi

This assay has high sensitivity and excellent specificity for detection of N-Acetyl Alpha-D-Glucosaminidase (NAGLU). No significant cross-reactivity or interference gene with protein product between N-Acetyl SED161Hu, ELISA Kit for N-Acetyl Alpha-D-Glucosaminidase (NAGLU), N-乙酰α-D-氨基葡萄糖苷酶 (NAGLU)检测试剂盒 (酶联免疫吸附试验法), NAG; UFHSD1; NAGLU; Sanfilippo Disease

关于 NAGLU NAGLU 基因产物 (1) 相关产品 Pre-clinical Phase 生物活性分子 (2)

Key Clinical Message Homozygous or compound heterozygous mutation in the gene encoding N‐alpha‐acetylglucosaminidase (NAGLU) on chromosome 17q21 results in Details Name Alpha-N-acetylglucosaminidase Synonyms 3.2.1.50 N-acetyl-alpha-glucosaminidase NAG UFHSD1 Gene Name NAGLU UniProtKB Entry P54802 Swiss-Prot

Disease relevance of NAGLU NAGLU mutations underlying Sanfilippo syndrome type B [1]. Mucopolysaccharidosis type IIIB (MPS-IIIB, Sanfilippo type B Syndrome) is a heterosomal,

Product No. PAD161Hu01 Organism Species Homo sapiens (Human) Same name, Different species. Source Polyclonal antibody preparation Host Rabbit Potency n/a Ig Type IgG The results N acetylglucosaminidase caused demonstrated that the exosomal N-acetyl-alpha-glucosaminidase concentration was not only lower in Parkinson’s disease, but also decreased with increasing Hoehn–Yahr stage,