Recombinant Human TGF-β1

Recombinant Human TGF-β1

Cat: PCH2537
★ ★ ★ ★ ★
规格:10μg 价格:¥2500
规格:50μg 价格:¥4000
规格:100μg 价格:¥6800

分类: 细胞因子 标签:

说明书 复制

产品名称

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 with ice bag. Upon receipt, store it immediately at the temperature listed below.

稳定性&储存

36 months at -20°C to -80°C in lyophilized state.6 months at -20°C to -80°C under sterile conditions after reconstitution.7-10 days at 2°C to 8°C under sterile conditions after reconstitution.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

 

蛋白活性

Measured in a cell inhibition assay using TF-1 cells at IL4 presence. 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.

 

 


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