ALG1 Antibody
-
货号:CSB-PA887118ESR2HU
-
规格:¥440
-
促销:
-
图片:
-
其他:
产品详情
-
产品名称:Rabbit anti-Homo sapiens (Human) ALG1 Polyclonal antibody
-
Uniprot No.:Q9BT22
-
基因名:ALG1
-
别名:4-mannosyltransferase antibody; Alg1 antibody; ALG1_HUMAN antibody; asparagine-linked glycosylation 1 homolog (yeast; beta-1,4-mannosyltransferase) antibody; asparagine-linked glycosylation 1; beta-1,4-mannosyltransferase homolog (S. cerevisiae) antibody; Asparagine-linked glycosylation protein 1 homolog antibody; Beta 1 4 mannosyltransferase antibody; Beta-1 antibody; CDG1K antibody; Chitobiosyldiphosphodolichol beta-mannosyltransferase antibody; GDP Man GlcNAc2 PP dolichol mannosyltransferase antibody; GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase antibody; GDP-mannose-dolichol diphosphochitobiose mannosyltransferase antibody; Hmat-1 antibody; HMAT1 antibody; HMT 1 antibody; HMT1 antibody; Mannosyltransferase 1 antibody; Mannosyltransferase-1 antibody; MT 1 antibody; MT-1 antibody; MT1 antibody
-
宿主:Rabbit
-
反应种属:Human
-
免疫原:Recombinant Human Chitobiosyldiphosphodolichol beta-mannosyltransferase protein (215-464AA)
-
免疫原种属:Homo sapiens (Human)
-
标记方式:Non-conjugated
-
克隆类型:Polyclonal
-
抗体亚型:IgG
-
纯化方式:Antigen Affinity Purified
-
浓度:It differs from different batches. Please contact us to confirm it.
-
保存缓冲液:PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
-
产品提供形式:Liquid
-
应用范围:ELISA, IHC
-
推荐稀释比:
Application Recommended Dilution IHC 1:20-1:200 -
Protocols:
-
储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
-
货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
-
功能:Participates in the formation of the lipid-linked precursor oligosaccharide for N-glycosylation. Involved in assembling the dolichol-pyrophosphate-GlcNAc(2)-Man(5) intermediate on the cytoplasmic surface of the ER.
-
基因功能参考文献:
- evaluated the genetic association of WDR3 and ALG1 in schizophrenia. We examined 21 single nucleotide polymorphisms [SNPs; W1 (rs1812607)-W16 (rs6656360), A1 (rs8053916)-A10 (rs9673733)] from these genes using the Japanese case-control sample (1,808 schizophrenics and 2,170 matched controls). No significant genetic associations of these SNPs were identified. However, we detected a significant association of W4 (rs319471) PMID: 29309433
- Study presents molecular, clinical and biochemical findings in the largest collection of ALG1-CDG cases ever reported at a single time with 39 cases, bringing the total number to 57. This ranks it the third most common CDG type behind PMM2-CDG and ALG6-CDG. In addition, highly lethal genotype were identified and confirm the presence of a unique xeno-tetrasaccharide in ALG1-CDG patients. PMID: 26931382
- In title. PMID: 25649379
- Was detected in the patient's ALG1-coding sequence. PMID: 24157261
- Family study defining the phenotype of deficiency of beta-1,4 mannosyltransferase (MT-1) congenital disorder of glycosylation (CDG), due to ALG1 gene mutations. Four novel ALG1 mutations were identified. PMID: 22966035
- DNA sequencing of ALG1 revealed nine different mutations, seven of which have not been previously reported. Clinical presentations of deficiency are severe, with dysmorphias, CNS involvement and ocular disturbances PMID: 20679665
显示更多
收起更多
-
相关疾病:Congenital disorder of glycosylation 1K (CDG1K)
-
亚细胞定位:Endoplasmic reticulum membrane; Single-pass type II membrane protein.
-
蛋白家族:Glycosyltransferase group 1 family, Glycosyltransferase 33 subfamily
-
数据库链接:
HGNC: 18294
OMIM: 605907
KEGG: hsa:56052
STRING: 9606.ENSP00000262374
UniGene: Hs.592086
Most popular with customers
-
Phospho-YAP1 (S127) Recombinant Monoclonal Antibody
Applications: ELISA, WB, IHC
Species Reactivity: Human
-
-
-
-
-
-
-