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| 产地 | France |
| 品牌 | AntibodySystem |
| 货号 | YHC92301 |
| 用途 | 仅用于科研 |
| 包装规格 | 100 μg |
| 纯度 | 0.95% |
| CAS编号 | |
| 是否进口 | 否 |
| 货号 | YHC92301 |
| 产品名称 | Recombinant Human COL6A2 Protein, N-His |
| 规格 | 100 μg |
| 价格 | 1880 |
| 状态 | Lyophilized |
| 储存缓冲液 | Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol. |
| 纯度 | >90% as determined by SDS-PAGE. |
| 应用 | ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress |
| 内毒水平 | Please contact with the lab for this information. |
| 表达系统 | E. coli |
| Accession | P12110 |
| 蛋白长度 | Phe671-Cys1019 |
| 预测分子量 | 41.47 kDa |
| 稳定性与储存条件 | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt. |
| 重悬 | Reconstitute in sterile water for a stock solution. |
| 别名 | COL6A2, Collagen alpha-2(VI) chain |
| 物种 | Homo sapiens (Human) |
| 运输 | In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise. |
| 备注 | For research use only. |
COL6A2为VI型胶原蛋白α2链,是构成细胞外基质的核心结构蛋白,广泛分布于人体多种结缔组织与肌肉组织。该蛋白可与其他胶原亚基组装形成VI型胶原纤维,维持组织结构完整性与力学稳定性,参与细胞黏附、基质重塑及组织修复过程,同时与肌肉组织稳态失调及基质微环境改变密切相关,是基质生物学及组织重构相关研究的重要靶点蛋白。
1.The UCMD-Causing COL6A1 (c.930 + 189C > T) Intron Mutation Leads to the Secretion and Aggregation of Single Mutated Collagen VI α1 Chains., PMID:40225172
2.Combined sequence and copy number analysis improves diagnosis of limb girdle and other myopathies., PMID:37688281
3.Identification and analysis of RNA-5-methylcytosine-related key genes in osteoarthritis., PMID:37700248
4.Single-cell communication patterns and their intracellular information flow in synovial fibroblastic osteoarthritis and rheumatoid arthritis., PMID:37704178
5.Exploration of diagnostic biomarkers, microenvironment characteristics, and ursolic acid's therapeutic effect for benign prostate hyperplasia., PMID:37705744
6.Unexpected partial RNA deletion by two different novel COL6A2 mutations leads to Ullrich congenital muscular dystrophy., PMID:37738610