ww.783成人A片,亚洲精品乱码久久久久久蜜桃91,www.71.com色婬免费,91午夜理伦私人影院
最近搜索:細胞培養(yǎng) 微生物學 分子生物 生物化學
首頁>>免疫學>>一抗>>骨保護蛋白配體/破骨細胞分化因子抗體
骨保護蛋白配體/破骨細胞分化因子抗體
  • 產(chǎn)品貨號:
    BN41584R
  • 中文名稱:
    骨保護蛋白配體/破骨細胞分化因子抗體
  • 英文名稱:
    Rabbit anti-RANKL/CD254 Polyclonal antibody
  • 品牌:
    Biorigin
  • 貨號

    產(chǎn)品規(guī)格

    售價

    備注

  • BN41584R-50ul

    50ul

    ¥1486.00

    交叉反應:Human,Mouse(predicted:Rat,Dog) 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

  • BN41584R-100ul

    100ul

    ¥2360.00

    交叉反應:Human,Mouse(predicted:Rat,Dog) 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

  • BN41584R-200ul

    200ul

    ¥3490.00

    交叉反應:Human,Mouse(predicted:Rat,Dog) 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

產(chǎn)品描述

英文名稱RANKL/CD254
中文名稱骨保護蛋白配體/破骨細胞分化因子抗體
別    名OPGL; CD254; hRANKL2; ODF; OPGL; Osteoclast differentiation factor; Osteoprotegerin ligand; RANKL; Receptor activator of nuclear factor kappa B ligand; sOdf; SOFA; TNF related activation induced cytokine; TNFSF 11; TNFSF11; TRANCE; Tumor necrosis factor ligand superfamily member 11; Osteoprotegerin Ligand; TNF11_HUMAN. 



研究領域腫瘤  細胞生物  免疫學  發(fā)育生物學  
抗體來源Rabbit
克隆類型Polyclonal
交叉反應Human, Mouse,  (predicted: Rat, Dog, )
產(chǎn)品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1μg/Test  IF=1:100-500 (石蠟切片需做抗原修復)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量35kDa
細胞定位細胞漿 細胞膜 分泌型蛋白 
性    狀Liquid
濃    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human OPGL:210-317/317 
亞    型IgG
純化方法affinity purified by Protein A
儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMedPubMed
產(chǎn)品介紹This gene encodes a member of the tumor necrosis factor (TNF) cytokine family which is a ligand for osteoprotegerin and functions as a key factor for osteoclast differentiation and activation. This protein was shown to be a dentritic cell survival factor and is involved in the regulation of T cell-dependent immune response. T cell activation was reported to induce expression of this gene and lead to an increase of osteoclastogenesis and bone loss. This protein was shown to activate antiapoptotic kinase AKT/PKB through a signaling complex involving SRC kinase and tumor necrosis factor receptor-associated factor (TRAF) 6, which indicated this protein may have a role in the regulation of cell apoptosis. Targeted disruption of the related gene in mice led to severe osteopetrosis and a lack of osteoclasts. The deficient mice exhibited defects in early differentiation of T and B lymphocytes, and failed to form lobulo-alveolar mammary structures during pregnancy. Two alternatively spliced transcript variants have been found. [provided by RefSeq, Jul 2008].

Function:
Cytokine that binds to TNFRSF11B/OPG and to TNFRSF11A/RANK. Osteoclast differentiation and activation factor. Augments the ability of dendritic cells to stimulate naive T-cell proliferation. May be an important regulator of interactions between T-cells and dendritic cells and may play a role in the regulation of the T-cell-dependent immune response. May also play an important role in enhanced bone-resorption in humoral hypercalcemia of malignancy.

Subcellular Location:
Cytoplasm; Secreted and Cell membrane.

Tissue Specificity:
Highest in the peripheral lymph nodes, weak in spleen, peripheral blood Leukocytes, bone marrow, heart, placenta, skeletal muscle, stomach and thyroid.

Post-translational modifications:
The soluble form of isoform 1 derives from the membrane form by proteolytic processing. The cleavage may be catalyzed by ADAM17.

DISEASE:
Defects in TNFSF11 are the cause of osteopetrosis autosomal recessive type 2 (OPTB2) [MIM:259710]; also known as osteoclast-poor osteopetrosis. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. The disorder occurs in two forms: a severe autosomal recessive form occurring in utero, infancy, or childhood, and a benign autosomal dominant form occurring in adolescence or adulthood. Autosomal recessive osteopetrosis is usually associated with normal or elevated amount of non-functional osteoclasts. OPTB2 is characterized by paucity of osteoclasts, suggesting a molecular defect in osteoclast development.

Similarity:
Belongs to the tumor necrosis factor family.

SWISS:
O14788

Gene ID:
8600

Database links:

Entrez Gene: 8600 Human

Entrez Gene: 21943 Mouse

Omim: 602642 Human

SwissProt: O14788 Human

SwissProt: O35235 Mouse

Unigene: 333791 Human

Unigene: 249221 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

OPGL骨保護蛋白配體又稱骨保護素配體(破骨細胞發(fā)育刺激因子)。屬腫瘤壞死因子TNF-a家族。
OPGL促進破骨細胞的分化和活性,而OPG抑制這些過程。骨髓瘤細胞影響骨髓中這兩種蛋白的生理平衡,是發(fā)生溶骨性病變的根本所在。


久久国产精品电影 | 人_禽—乱—交—视—频 | 四川BBB揉BBB揉多人乱薍 | 俄罗斯无码成人午夜电影 | 精品国婬伦v无码久久久黑人 | 中文字幕无码在线观看视频 | 久久免费观看视频 | 无码人妻久久久午夜一区二区三区 | 免费一级A片刺激高潮 | 高清无码在线观看视频 | 成人人人人人欧美片做爰 | 西西4444WWW大胆无视频双腿 | 四川婬片A片AAA片真人 | 国产乱码日产乱码精品精 | 午夜亚洲福利在线老司机 | 一级a免一级a做免费线看内裤游戏 | 老司机午夜福利视频 | 波多野结衣午夜福利 | 国产偷窥熟妇高潮呻吟 | 午夜成人理论片A片AAA图片 | 91极品美女裸身网站直播 | 无码人妻一区二区三区线花季软件 | 成人一区二区三中文破解版新视 | 国产自产精品一区精品 | 国产日韩欧美高潮无码一区二区 | 人妻少妇被猛烈进入中文字幕 | 无人码人妻一区二区三区免费 | 真人一级毛片免费 | 日本少妇一区二区三区 | 久久精品一区二区三区不卡牛牛 | 国产美女无遮挡在线观看 | 久热这里只有精品伦理片 | 西西4444WWW无码精品 | 亚欧精品无码7777视频 | 国产一级特黄AAA片奶水流 | 不卡的av在线四季Aⅴ | 老熟女亂伦一区二区三区在线 | 人妻少妇被猛烈进入中文字幕 | 人妻无码久久精品人妻 | 亚洲国产精品综合久久99视频 | 国产黄色视频在线观看 |