Analytical Data
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基因名
CD40L/CD154/TRAP
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简介
CD40L (CD154; TRAP) is a ligand to CD40/TNFRSF5, acts function by generating a costimulatory signal that up-regulates IL-4 synthesis[1]. CD40L is specifically expressed on activated CD4+ T-lymphocytes and involves in activation of NF-κB/MAPK pathway[2][3]. CD40L also involves in B cell differentiation, maturation, and apoptosis[4]. CD40L in human, cleaved into 2 chains of membrane form (1-261 a.a.) and soluble form (113-261 a.a.) which serves as a ligand for integrins (ITGA5:ITGB1 and ITGAV:ITGB3). CD40L/CD154/TRAP Protein, Human (HEK293, hFc-Flag) has a total length of 248 amino acids (M13-L261), is expressed in HEK392 cells with N-terminal hFc- and Flag-tag.
- Application
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生物活性
1.Measured by its binding ability in a functional ELISA. Immobilized CD40L at 2 μg/mL can bind Anti-CD40L Rabbit Monoclonal Antibody, the EC50 is ≤3.3 ng/mL. 2.Measured by its binding ability in a functional ELISA. Immobilized CD40 at 2 μg/mL can bind CD40L, the EC50 is 3.112-3.858 ng/mL. 3.Human CD40 protein hFc tag captured on COOH chip can bind Human CD40L protein hFc and Flag tag with an affinity constant < 2.06 nM as detected by LSPR Assay. 4. Immobilized Human CD40 Ligand Trimer, His Tag at 1 μg/mL (100 μl/Well) on the plate. Dose response curve for Human CD40, hFc Tag with the EC50 of 1.29 μg/mL determined by ELISA. 5.Measured in a cell proliferation assay using human B cells (Ramos) in the presence of 10 ng/mL Human IL-4 (HY-P70445). The ED50 for this effect is 2.718 ng/mL, corresponding to a specific activity is 3.679×105 units/mg. Measured in a cell proliferation assay using human B cells (Ramos) in the presence of 10ng/mL Human IL-4 (HY-P70445). The ED50 for this effect is 2.718 ng/mL, corresponding to a specific activity is 3.679×105 units/mg.
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别名
CD40-L; T-cell antigen Gp39; NF-related activation protein; TRAP; Tumor necrosis factor ligand superfamily member 5; CD154; sCD40L;
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种属
Human
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表达系统
HEK293
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标签
N-hFc;N-Flag
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
P29965
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表达区间
M113-L261
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蛋白长度
Full Length of CD40L soluble form
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分子量
44-50 kDa.
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内毒素
< 1.0 EU per μg protein as determined by the LAL method.
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性状
Freeze-dried powder
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缓冲液
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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复溶方法
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- 个性化定制
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稳定性测试
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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保存条件 & 期限
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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运输条件
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
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Protein Description
CD40L, also known as CD154, is a crucial membrane protein primarily expressed on activated T cells and plays a pivotal role in immune system regulation by providing essential signals to B cells and other antigen-presenting cells through CD40 receptor engagement. This interaction is vital for processes such as B cell activation, proliferation, and isotype switching, all of which are fundamental for generating effective adaptive immune responses. In addition, CD40L is implicated in various immunological disorders, including autoimmune diseases and cancers, making it an attractive target for therapeutic interventions. To study its functions and potential applications, researchers have developed recombinant CD40L proteins, often referred to as TRAP (trimeric association protein), which can mimic the natural signaling of CD40L. These recombinant proteins facilitate the investigation of CD40/CD40L pathways in controlled settings, enabling the exploration of their roles in immune responses and paving the way for innovative treatments that harness this pathway. Understanding the structure and function of CD40L/TRAP enhances our knowledge of immune mechanisms and could lead to novel strategies for modulating immune responses in various diseases.












