PDL1 Fc Chimera, Human
型号:null    产品货号: CB055-2952
价格:请致电:010-57128832,18610462672
品牌: 美国

Programmed death-ligand 1 (PD-L1) also known as cluster of differentiation 274 (CD274) or B7 homolog 1 (B7-H1), is a protein that in humans is encoded by the CD274 gene. PD-L1 is a 40 kDa type 1 transmembrane protein that has been speculated to play a major role in suppressing the immune system during particular events such as pregnancy, tissue allografts, autoimmune disease and other disease states such as hepatitis. Normally the immune system reacts to foreign antigens where there is some accumulation in the lymph nodes or spleen which triggers a proliferation of antigen-specific CD8+ T cell. The formation of PD-1 receptor / PD-L1 or B7.1 receptor /PD-L1 ligand complex transmits an inhibitory signal which reduces the proliferation of these CD8+ T cells at the lymph nodes and supplementary to that PD-1 is also able to control the accumulation of foreign antigen specific T cells in the lymph nodes through apoptosis which is further mediated by a lower regulation of the gene Bcl-2. PD-L1 binds to its receptor, PD-1, found on activated T cells, B cells, and myeloid cells, to modulate activation or inhibition.     
Recombinant Human PD-L1(B7-H1) Fc Chimera produced in CHO cells is a polypeptide chain containing 457 amino acids. A fully biologically active molecule, rh PDL1(B7-H1) has a molecular mass of 70-72 kDa analyzed by reducing SDS-PAGE and is obtained by chromatographic techniques at ExCell Bio.

制剂是一种蛋白酶抑制剂,其功能是抑制补体系统,以防止过度活化或自发活化。该抑制作用是通过结合并不可逆地抑制C1复合物中的C1r和C1s蛋白酶而实现的,最终导致补体激活级联反应中的所有下游事件均被关闭。补体C1抑制剂也能抑制多种其它蛋白酶,如激肽释放酶Kallikrein,因子XIa和因子XIIa。补体C1抑制剂的缺乏是遗传性血管水肿(HAE,遗传性血管神经性水肿)的主要病因,此疾病的主要特征是呼吸道和胃肠道的水肿。临床上,直接注射补体C1抑制剂有时可用于治疗HAE以及其它一些病症。重组人补体C1抑制剂是高度糖基化的蛋白,含有455个氨基酸残基(分子量为49.4kDa),对应于补体C1抑制剂前体的56-500位氨基酸。该重组人补体C1抑制剂对C1复合物具有完全的抑制作用。糖基化的补体C1抑制剂,在还原型SDS-PAGE分析中的表观分子量约为80-90 kDa。
AA Sequence:
VEPILEVSSL PTTNSTTNSA TKITANTTDE PTTQPTTEPT TQPTIQPTQP TTQLPTDSPT QPTTGSFCPG PVTLCSDLES HSTEAVLGDA LVDFSLKLYH AFSAMKKVET NMAFSPFSIA SLLTQVLLGA GENTKTNLES ILSYPKDFTC VHQALKGFTT KGVTSVSQIF HSPDLAIRDT FVNASRTLYS SSPRVLSNNS DANLELINTW VAKNTNNKIS RLLDSLPSDT RLVLLNAIYL SAKWKTTFDP KKTRMEPFHF KNSVIKVPMM NSKKYPVAHF IDQTLKAKVG QLQLSHNLSL VILVPQNLKH RLEDMEQALS PSVFKAIMEK LEMSKFQPTL LTLPRIKVTT SQDMLSIMEK LEFFDFSYDL NLCGLTEDPD LQVSAMQHQT VLELTETGVE AAAASAISVA RTLLVFEVQQ PFLFVLWDQQ HKFPVFMGRV YDPRA
Source:
CHO cells
Purity:
Greater than 95% by SDS-PAGE gel and HPLC analyses.
Biological Activity:
Measured by its ability to inhibit recombinant human complement component C1a cleavage of a colorimetric peptide substrate, N Carbobenzyloxy-Lys-ThioBenzyl ester (Z-K-SBzl).  The expected IC50 is ≤ 2.6 nM.
 
 
 
 
Research Interests:
ApoptosisApoptosisImmune SystemImmune System
InflammationInflammation 
 
 
Country of Origin:
USA
Research Use Only. Not for use in diagnostic or therapeutic procedures.