Cell Signaling Technology

Product Pathways - Growth Factors/Cytokines

Human His6BAFF/TNFSF13B (hHis6 BAFF) #5413

B lymphocyte stimulator   B-cell-activating factor   BAF   BAF complex   BAFF complex   BLyS   Dendritic cell-derived TNF-like molecule   his tag   TALL-1   TNF- and APOL-related leukocyte expressed ligand 1   Tumor necrosis factor ligand superfamily member 13B  

No. Size Price
5413LC 50 µg ( With Carrier ) ¥7,984.00 现货查询 购买询价 防伪查询
5413LF 50 µg ( Carrier Free ) ¥7,984.00 现货查询 购买询价 防伪查询
5413SC 10 µg ( With Carrier ) ¥2,644.00 现货查询 购买询价 防伪查询
5413SF 10 µg ( Carrier Free ) ¥2,644.00 现货查询 购买询价 防伪查询
5413 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype

Species cross-reactivity is determined by western blot.

Applications Key:

Source / Purification

Recombinant human His6BAFF (hHis6BAFF) Ala134-Leu285 (Accession #NP_006564) was expressed in human 293 cells at Cell Signaling Technology.

CST公司生产的人重组蛋白His6BAFF (hHis6BAFF) Ala134-Leu285 (Accession #NP_006564)是从人的293细胞表达而来。

Molecular Characterization

Recombinant N-terminally His6-tagged hBAFF has a calculated MW of 18,066. DTT-reduced and non-reduced protein migrate as 21 kDa polypeptides. The expected amino terminus of recombinant hHis6BAFF was verified by amino acid sequencing.



>98% as determined by SDS-PAGE of 6 μg reduced (+) and non-reduced (-) recombinant hHis6BAFF. All lots are greater than 98% pure.

6 μg 还原 (+) 和 非还原的(-) 重组hHis6BAFF通过SDS-PAGE检测,纯度大于98%,所有批次的纯度均高于98%。


The bioactivity of recombinant hHis6BAFF was determined in a cell proliferation assay using mouse splenic B cells. The ED50 of each lot is between 0.5-2 ng/ml.

hHis6BAFF的生物活性是通过诱导小鼠脾细胞增值能力的实验来确定的。每个批次的ED50在0.5-2 ng/ml之间。

Coomassie Gel

Coomassie Gel

The purity of recombinant hHis6BAFF was determined by SDS-PAGE of 6 µg reduced (+) and non-reduced (-) recombinant hHis6BAFF and staining overnight with Coomassie Blue.重组 hHis6BAFF 蛋白的纯度通过SDS-PAGE 来确定。6 µg 经还原(+)和未经过还原(-) 的重组 hHis6BAFF 蛋白跑SDS胶并用考马斯亮蓝染色过夜。



The proliferation of mouse splenic B cells treated with increasing concentrations of hHis6BAFF in the presence of 10 μg/ml of goat anti-mouse IgM μ chain was assessed. After 72 hour treatment with hHis6BAFF, cells were incubated with a tetrazolium salt and the OD450-OD650 was determined.在10 μg/ml羊抗鼠IgM μ 链存在下用递增浓度的hHis6BAFF处理小鼠脾B细胞并观察其增值的实验。用hHis6BAFF培养细胞72小时后与四唑盐孵育并测定 OD450-OD650 数值。

Western Blotting

Western Blotting

Western blot analysis of extracts from mouse splenic B cells, untreated or treated with hHis6BAFF for 24 hours, using Phospho-p44/42 MAPK (Erk1/2) (Thr202/Tyr204) (D13.14.4E) XP® Rabbit mAb #4370 (upper) and p44/42 MAPK (Erk1/2) (137F5) Rabbit mAb #4695 (lower).Western免疫印迹。用Phospho-p44/42 MAPK (Erk1/2) (Thr202/Tyr204) (D13.14.4E) XP® Rabbit mAb #4370(上图)和p44/42 MAPK (Erk1/2) (137F5) Rabbit mAb #4695 (下图) 研究未经处理的和经hHis6BAFF处理24小时的小鼠脾细胞的细胞提取液。


Less than 0.01 ng endotoxin/1 μg hHis6BAFF.

每微克hHis6BAFF内毒素含量小于0.01 ng。


With carrier: Lyophilized from a 0.22 μm filtered solution of PBS, pH 7.2 containing 10 mM DTT and 20 μg BSA per 1 μg hHis6BAFF. Cystines are not required for bioactivity. Carrier free: Lyophilized from a 0.22 μm filtered solution of PBS, pH 7.2 containing 10 mM DTT. Cystines are not required for bioactivity.

有载体: 每微克hHis6BAFF蛋白溶解在包含10 mM DTT和20 μg BSA的PBS(pH 7.2)溶液中,并通过 0.22 μm 滤膜冻干,胱氨酸不是生物活性所需要的。

无载体:每微克hHis6BAFF蛋白溶解在包含10 mM DTT的PBS(pH 7.2)溶液,并通过 0.22 μm 滤膜冻干,胱氨酸不是生物活性所需要的。


BAFF, a member of the TNF superfamily of proteins, is a homotrimeric transmembrane protein, which is cleaved to produce a soluble cytokine (1). BAFF may also further oligomerize into 60-mer structures (1). BAFF is expressed by neutrophils, macrophages, dendritic cells, activated T cells, and epithelial cells (1,2). BAFF plays a key role in B cell development, survival, and activation (1,3,4). BAFF binds to three distinct receptors, BAFF-R, TACI, and BCMA (1). These receptors are differentially expressed during B cell development and among B cell subsets (1,2,4). While BAFF-R and BCMA bind to the homotrimeric form of BAFF, TACI only binds to membrane-bound or higher order BAFF structures (1). The BAFF/ BAFF-R interaction activates both canonical and non-canonical NF-κB pathways, PI3K/Akt, and mTor signaling (2,4). Activation of the noncanonical NF-κB pathway via BAFF-R is negatively regulated by TRAF3 (5). Elevated levels of BAFF may exacerbate many autoimmune disorders, making it an attractive therapeutic target (2).

BAFF, TNF超家族的蛋白成员,是一个同源三聚体跨膜蛋白,经过剪切后可以形成可溶性的细胞因子(1)。BAFF 也能进一步的聚合形成60聚体结构(1)。BAFF在中性粒细胞、巨噬细胞、树突状细胞、活化的T细胞和上皮细胞中表达(1,2)。BAFF 在B细胞的发育、存活和激活中发挥了主要的作用(1,3,4)。BAFF结合到3个不同的受体上—BAFF-R、TACI 和 BCMA (1)。这些受体在B细胞及其谱系细胞的发育中具有不同的表达形式(1,2,4)。不像BAFF-R 和BCMA只结合到BAFF的三聚体形式上, TACI只能结合到细胞膜上或者BAFF更高级的结构上(1)。BAFF/ BAFF-R 的相互作用激活典型和非典型的NF-κB信号通路, PI3K/Akt 和 mTOR (2,4)。通过BAFF-R激活非典型的NF-κB信号通路受到TRAF3负调控(5)。研究表明BAFF水平的升高可能加剧许多自身免疫性疾病,这使得它成为治疗的理想靶标(2)。

Application References

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For Research Use Only. Not For Use In Diagnostic Procedures.

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.

Cell Signaling Technology® is a trademark of Cell Signaling Technology, Inc.

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