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RecombinantProteins
重組蛋白

Rat / Mouse TGF-beta 1 / TGFB1 Protein/重組大鼠/小

發(fā)布時間:2024-07-31 16:13:56

名稱

Rat / Mouse TGF-beta 1 / TGFB1 Protein/重組大鼠/

規(guī)格

20ug

編號

CZDB-014

價格

詢價

中文名

Rat / Mouse TGF-beta 1 / TGFB1 Protein/重組大鼠/

分子別稱

TGFB1

分子種屬

Mouse

表達標簽

His,S

表達宿主

E. coli

濃度

> 95 % as determined by SDS-PAGE

緩沖液

Lyophilized from sterile PBS, pH 7.4

存儲條件

-70°C,應避免反復凍融。

基本描述

TGF-beta 1 is a member of the transforming growth factor beta (TGF-beta) family. The transforming growth factor-beta family of polypeptides are involved in the regulation of cellular processes, including cell division, differentiation, motility, adhesion and death. TGF-beta 1 positively and negatively regulates many other growth factors. It inhibits the secretion and activity of many other cytokines including interferon-γ, tumor necrosis factor-alpha and various interleukins. It can also decrease the expression levels of cytokine receptors. Meanwhile, TGF-beta 1 also increases the expression of certain cytokines in T cells and promotes their proliferation, particularly if the cells are immature. TGF-beta 1 also inhibits proliferation and stimulates apoptosis of B cells, and plays a role in controlling the expression of antibody, transferrin and MHC class II proteins on immature and mature B cells. As for myeloid cells, TGF-beta 1can inhibit their proliferation and prevent their production of reactive oxygen and nitrogen intermediates. However, as with other cell types, TGF-beta 1 also has the opposite effect on cells of myeloid origin. TGF-beta 1 is a multifunctional protein that controls proliferation, differentiation and other functions in many cell types. It plays an important role in bone remodeling as it is a potent stimulator of osteoblastic bone formation, causing chemotaxis, proliferation and differentiation in committed osteoblasts. Once cells lose their sensitivity to TGF-beta1-mediated growth inhibition, autocrine TGF-beta signaling can promote tumorigenesis. Elevated levels of TGF-beta1 are often observed in advanced carcinomas, and have been correlated with increased tumor invasiveness and disease progression.