97久久久精品综合88久久_亚洲国产精品一_久热热国产久热_97操操操_北条麻妃在线免费观看_精品国自产拍天天拍

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
欧美人妻久久精品,俄罗斯一级黄色毛片,成人综合久久综合
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Haptoglobin/BF594 Conjugated antibody (bs-1808R-BF594)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-1808R-BF594
英文名稱 Rabbit Anti-Haptoglobin/BF594 Conjugated antibody
中文名稱 BF594標記的結合珠蛋白/觸珠蛋白抗體
別    名 haptoglobin; Bp; Haptoglobin alpha chain; Haptoglobin alpha(1S) beta; Haptoglobin alpha(2FS) beta; Haptoglobin beta chain; Haptoglobin, alpha polypeptide; Haptoglobin, beta polypeptide; HP; Hp2 alpha; HP2 ALPHA2; HPA1S; HPT; MGC111141; HPT_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  免疫學  生長因子和激素  激酶和磷酸酶  結合蛋白  糖蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 27/43kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Haptoglobin beta chain
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 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產品介紹 background:
This gene encodes a preproprotein, which is processed to yield both alpha and beta chains, which subsequently combine as a tetramer to produce haptoglobin. Haptoglobin functions to bind free plasma hemoglobin, which allows degradative enzymes to gain access to the hemoglobin, while at the same time preventing loss of iron through the kidneys and protecting the kidneys from damage by hemoglobin. Mutations in this gene and/or its regulatory regions cause ahaptoglobinemia or hypohaptoglobinemia. This gene has also been linked to diabetic nephropathy, the incidence of coronary artery disease in type 1 diabetes, Crohn's disease, inflammatory disease behavior, primary sclerosing cholangitis, susceptibility to idiopathic Parkinson's disease, and a reduced incidence of Plasmodium falciparum malaria. A similar duplicated gene is located next to this gene on chromosome 16. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Function:
As a result of hemolysis, hemoglobin is found to accumulate in the kidney and is secreted in the urine. Haptoglobin captures, and combines with free plasma hemoglobin to allow hepatic recycling of heme iron and to prevent kidney damage. Haptoglobin also acts as an Antimicrobial; Antioxidant, has antibacterial activity and plays a role in modulating many aspects of the acute phase response. Hemoglobin/haptoglobin complexes are rapidely cleared by the macrophage CD163 scavenger receptor expressed on the surface of liver Kupfer cells through an endocytic lysosomal degradation pathway.
Uncleaved haptoglogin, also known as zonulin, plays a role in intestinal permeability, allowing intercellular tight junction disassembly, and controlling the equilibrium between tolerance and immunity to non-self antigens.

Subunit:
Tetramer of two alpha and two beta chains; disufide-linked. The Hemoglobin/haptoglobin complex is composed of a haptoglobin dimer bound to two hemoglobin alpha-beta dimers. Interacts with CD163.

Subcellular Location:
Secreted.

Tissue Specificity:
Expressed by the liver and secreted in plasma.

DISEASE:
Anhaptoglobinemia (AHP) [MIM:614081]: A condition characterized by the absence of the serum glycoprotein haptoglobin. Serum levels of haptoglobin vary among normal persons: levels are low in the neonatal period and in the elderly, differ by population, and can be influenced by environmental factors, such as infection. Secondary hypohaptoglobinemia can occur as a consequence of hemolysis, during which haptoglobin binds to free hemoglobin. Congenital haptoglobin deficiency is a risk factor for anaphylactic non-hemolytic transfusion reactions. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the peptidase S1 family. Contains 1 peptidase S1 domain. Contains 2 Sushi (CCP/SCR) domains.

Database links:

Entrez Gene: 3240 Human

Entrez Gene: 15439 Mouse

Entrez Gene: 24464 Rat

Omim: 140100 Human

SwissProt: P00738 Human

SwissProt: Q61646 Mouse

SwissProt: P06866 Rat

Unigene: 513711 Human

Unigene: 702099 Human

Unigene: 26730 Mouse

Unigene: 10950 Rat



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

haptoglobin是一種酸性糖蛋白,屬α2唾液酸糖蛋白,主要由肝臟合成,也可在脂肪細胞、皮膚、脾、肌肉、肺內等合成。
版權所有 2004-2026 www.kastlife.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 波多野结衣伦理在线观看 | 免费国产片 | 久久精品美女 | 欧美肥老太交性506070 | 二次元人物桶二次元人物免费 | 蜜桃av资源| 日本最新在线观看一区二区三区 | 中文字幕久精品免费视频 | ww939766com永久免费 | 爆乳无码中文字幕在线观看 | 国产三级精品三级在专区 | 啊灬啊灬啊灬快灬高潮了听书 | 伊人狠狠干 | 日本在线综合 | JAPAN黑人极大黑炮 | 国产精品色在线 | 67194成在线观看免费 | 久久久国产三级 | 午夜精品二区 | 久久好色视频 | 国产黑丝美女av | av免费播放网址 | 美女胸18下看禁止免费视频51 | 精品剧情V国产在线观看 | 中文字幕人妻丝袜成熟乱 | 9191视频 | 久久久久人妻精品区一三寸 | 蜜臀久久精品久久久久久酒店? | 日韩中文字幕一区二区三区 | 九九热线视频只有这里最精品 | 亚洲精品乱码久久久久久不卡 | 毛片免费视频播放 | 天天看天天射 | 国产欧美日韩另类色视频云霸 | 18国产精品福利片久久婷 | AV人摸人人人澡人人超碰手机版 | 久久精品无码专区免费东京热 | 亚洲国产播放 | 我要看黄色大片 | 婷婷久久综合九色综合88 | 少妇在宾馆高潮不断狂叫床 |