提供的GGCX人源重组蛋白(Q01)产品为带有GST标签的人源GGCX部分序列重组蛋白,其对应的GeneID号为2677。 产品描述 与其它公司提供的重组蛋白不同,该GGCX人源重组蛋白(Q01)产品为采用CFS的无细胞麦胚蛋白合成系统表达出来的重组蛋白,可表达出对细胞有毒性、易被蛋白酶降解的蛋白;并获得具有良好的可溶性,并有翻译后修饰...
基因简称(symbol) GGCX [HGNC] [GeneCards] [NCBI] 基因种类(locus group) protein-coding gene 同源简称(alias symbol) VKCFD1 基因家族代码(gene_family_id) [HGNC] [GenScript] omim代码 137167 entrez码 2677 [Vega] vega基因码 OTTHUMG00000130173 ensembl基因码 ENSG00000115486 [Ensembl] ...
软骨,关节骨关节炎GGCX基因基质金属蛋白酶13Objective To research the effect of GGCX gene on MMP13 in rabbit osteoarthritis cartilage cells and investigate its effect on osteoarthritis cartilage degeneration.Methods Six Japanese big ear rabbits weighted (2.0±0.2)kg were randomly di vided into three ...
Gene ID: 2677 种属 Homo sapiens DNA序列编号: NM_000821.7 DNA描述 Homo sapiens gamma-glutamyl carboxylase (GGCX), transcript variant 1, mRNA DNA大小: 7556 bp DNA编码区: atggcggtgtctgccgggtccgcgcggacctcgcccagctcagataaagtacagaaagac aaggctgaactgatctcagggcccaggcaggacagccgaatagggaaactcttgggtttt ...
关键词:新疆地区;哈萨克族;汉族;GGCX;rsl1676382;rs6751560;基因多态性中图分类号:541.4文献标识码:A文章编号:1009—5551(2014)10-I289—05doJ:10.3969/j.issn.1009—5551.2014.10.011AnalysisofGGCXgenepolymorphisminKazakh,HanpopulationinXinjiangareaXiayizhaKmali,MUHuyati,LUWuhong,LIUZhiqiang,HEPengyi,YANGYuchun(...
Results Eighty patients were enrolled in this research, and two types of genewere found, including CYP2C9*1*1 in 73 patients and CYP2C9*1*3 in 7 patients. For gene, therewere 42 *A*G patients and 38 GGCX*G*G patients. There was no significant difference between thetwo groups in ...
Gene ID: 四千零九十二 数据库链接: Enter Z基因:4092人 Entrez Gene:17131只老鼠 Entrez Gene:81516只老鼠 Omim:602932个人 SwissProt:O15105人类 SwissProt:O35253小鼠 SwissProt:O88 406大鼠 Unigne:465087人 重要注意事项: 所提供的产品仅用于研究用途,不用于人体、治疗或诊断应用。
Compound heterozygous mutations in the gamma-glutamyl carboxylase gene cause combined deficiency of all vitamin K-dependent blood coagulation factors. Summary Hereditary combined deficiency of the vitamin K-dependent coagulation factors II, VII, IX, X, protein C, S and protein Z (VKCFD) is a very...
Gene Symbol GGCX Gene ID (NCBI) 2677 RRID AB_2110874 Conjugate Unconjugated Form Liquid Purification Method Antigen affinity purification UNIPROT ID P38435 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...
The classic forms of PXE are caused by mutations in the ABCC6 gene encoding the ABCC6 protein expressed primarily in the liver. Cutis laxa (CL) manifests with loose and sagging skin with loss of recoil. In 2009 we investigated a 19-year-old patient with overlapping cutaneous features of ...