武汉恩玑生命科技有限公司
菜单 Close 公司首页 公司介绍 公司动态 证书荣誉 联系方式 在线留言
您当前的位置: 网站首页 > 产品展厅 >细胞辅助试剂 >细胞因子 >GMP Recombinant Human TGF-β1
产品展厅
GMP Recombinant Human TGF-β1
  • 品牌:EnkiLife
  • 产地:中国
  • 型号:
  • 货号:PCH90040
  • 价格: ¥2500/10μg
  • 发布日期: 2024-11-30
  • 更新日期: 2025-05-22
产品详请
产地 中国
保存条件
品牌 EnkiLife
货号 PCH90040
用途 细胞培养用细胞因子
组织来源
细胞形态
是否是肿瘤细胞
保质期
器官来源
免疫类型
品系
生长状态
物种来源
包装规格
是否进口
产品名称

GMP Recombinant Human TGF-β1

蛋白名

TGF-β1

纯度

Greater than 95% as determined by reducing SDS-PAGE

内毒素

≤10 EU/mg

蛋白构建

Recombinant Human TGF-β1 is produced by our Mammalian cell expression system and the target gene encoding Ala279-Ser390 is expressed.

Accession #

P01137

蛋白标签

Tag free

表达宿主

Mammalian cell

种属

Human

预测分子量

12.8 kDa

蛋白形态

Lyophilized

储存缓冲液

0.085% TFA,30% ACN,5% mannitol,pH 2.5

运输方式

The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature listed below.

稳定性&储存

Store at ≤-70°C, stable for 6 months after receipt. Store at ≤-70°C, stable for 43 months under sterile conditions after opening. Please minimize freeze-thaw cycles.

复溶

Always centrifuge tubes before opening. Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100μg/ml. Dissolve the lyophilized protein in distilled water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles.

 

 

 

分子别名

Transforming Growth Factor Beta-1; TGF-Beta-1; Latency-Associated Peptide; LAP; TGFB1; TGFB

 

Bioactivity

The ED50 for this effect is ≤0.1ng/mL.

 

背景介绍

Transforming Growth Factor β-1 (TGFβ-1) is a secreted protein which belongs to the TGF-β family. TGFβ-1 is abundantly expressed in bone, articular cartilage and chondrocytes and is increased in osteoarthritis (OA). TGFβ-1 performs many cellular functions, including the control of cell growth, cell proliferation, cell differentiation and apoptosis. The precursor is cleaved into a latency-associated peptide (LAP) and a mature TGFβ-1 peptide.Disulfide-linked homodimers of LAP and TGF-beta 1 remain non-covalently associated after secretion, forming the small latent TGF-beta 1 complex. Purified LAP is also capable of associating with active TGF-beta with high affinity, and can neutralize TGF-beta activity. Covalent linkage of LAP to one of three latent TGF-beta binding proteins (LTBPs) creates a large latent complex that may interact with the extracellular matrix. TGF-beta activation from latency is controlled both spatially and temporally, by multiple pathways that include actions of proteases such as plasmin and MMP9, and/or by thrombospondin 1 or selected integrins. Although different isoforms of TGF-beta are naturally associated with their own distinct LAPs, the TGF-beta 1 LAP is capable of complexing with, and inactivating, all other human TGF-beta isoforms and those of most other species. Mutations within the LAP are associated with Camurati-Engelmann disease, a rare sclerosing bone dysplasia characterized by inappropriate presence of active TGF-beta 1.