One-stop service from gene synthesis and vector construction to protein expression and purification. Multiple protein expression systems: bacterial, yeast, baculovirus-insect and mammalian expression system. Multiple purification systems (30+) to choose. ...
CDS-H04600-1 pDonR223-FAM126A GateWay 2ug/0.5ml ￥800 现货 CDS-H04600-2 pMD18-T-FAM126A TA克隆 2ug/0.5ml ￥800-1500 1-2周FAM126A 重组腺病毒 货号产品名称Method规格价格货期 CDS-H04600-11 rAd-FAM126A 重组过表达腺病毒 10^10 vg/支 ￥2500 3-5周 CDS-H04600-12 rAd-sh-FA...
Gene ID (NCBI) 84668 RRID AB_2880443 Conjugate Unconjugated Form Liquid Purification Method Antigen affinity purification UNIPROT ID Q9BYI3 Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3. Storage Conditions Store at -20°C. Stable for one year after shipment. Aliquoting is...
MyelinationWhite matter disorderCataractFAM126A geneHypomyelination and congenital cataract (HCC, OMIM #610532) is a rare autosomal recessive disorder due to FAM126A mutations characterized by congenital cataract, progressive neurologic impairment, and myelin deficiency in the central and peripheral ...
Entrez Gene ID: (Human) 84668, (Mouse) 84652 功能 signal transducer activity protein binding molecular_function 参与通路 biological_process signal transduction myelination phosphatidylinositol phosphorylation establishment of protein localization to plasma membrane 性能保障 只要您发现Invitrogen抗体在实验中的...
Target NameFAM126A Accession No.Swiss-Prot:Q9BYI3 Gene ID:84668 UniprotQ9BYI3 Gene ID84668; Concentration1mg/ml FormulationSupplied in 0.1M Tris-buffered saline with 10% Glycerol (pH7.0). 0.01% Thimerosal was added as a preservative.
Hypomyelination and congenital cataract (HCC), one of these disorders, is caused by mutations in FAM126A, a gene of unknown function3. We show that FAM126A, also known as hyccin, regulates the synthesis of phosphatidylinositol 4-phosphate (PtdIns(4)P), a determinant of plasma membrane ...
查看其他5个FAM126A抗体 说明书 实验方案 技术支持 货号PA5-34761 CNY4,312.00 100 µL 下单后预计有货时间 14-Apr-2025 查看价格 批量或定制请求 Application Created with Sketch. 图:1/2 FAM126A Antibody (PA5-34761) in WB Western Blot using FAM126A Polyclonal Antibody (Product # PA5-34761...
The gene responsible for an autosomal recessive Pelizaeus-Merzbacher-like disease called HLD5 is named fam126a (also known as hyccin or drctnnb1a). While the gene mutations often cause FAM126A protein deficiency, one known missense mutation, Leu-53-to-Pro (L53P), allows some protein to...
Target Description: FAM126A may play a part in the beta-catenin/Lef signaling pathway. Expression of FAM126A gene is down-regulated by beta-catenin. Defects in FAM126A gene are a cause of hypomyelination with congenital cataract (HCC). ...