强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
掃碼關(guān)注公眾號(hào)           掃碼咨詢(xún)技術(shù)支持           掃碼咨詢(xún)技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
91亚洲精品国偷拍自产在线观看 ,国产熟妇婬乱A片免费看牛牛
首頁(yè) > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
DLAT Rabbit pAb (bs-19695R)  
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@bioss.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢(xún)價(jià)

產(chǎn)品編號(hào) bs-19695R
英文名稱(chēng) DLAT Rabbit pAb
中文名稱(chēng) 丙酮酸脫氫酶E2抗體
別    名 ODP2_HUMAN; Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial; EC:2.3.1.12; 70 kDa mitochondrial autoantigen of primary biliary cirrhosis(PBC); Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex; M2 antigen complex 70 kDa subunit; Pyruvate dehydrogenase complex component E2(PDC-E2; PDCE2); dihydrolipoamide S-acetyltransferase; E2; PBC; DLTA; PDCE2; PDC-E2;  
研究領(lǐng)域 腫瘤  細(xì)胞生物  神經(jīng)生物學(xué)  新陳代謝  線粒體  
抗體來(lái)源 Rabbit
克隆類(lèi)型 Polyclonal
交叉反應(yīng) Human,Mouse,Rat,Zebrafish (predicted: Rabbit,Pig,Sheep,Cow,Dog,Cat,GuineaPig,Horse)
產(chǎn)品應(yīng)用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 63 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞漿 線粒體
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PDCE2: 231-330/647 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 This gene encodes component E2 of the multi-enzyme pyruvate dehydrogenase complex (PDC). PDC resides in the inner mitochondrial membrane and catalyzes the conversion of pyruvate to acetyl coenzyme A. The protein product of this gene, dihydrolipoamide acetyltransferase, accepts acetyl groups formed by the oxidative decarboxylation of pyruvate and transfers them to coenzyme A. Dihydrolipoamide acetyltransferase is the antigen for antimitochondrial antibodies. These autoantibodies are present in nearly 95% of patients with the autoimmune liver disease primary biliary cirrhosis (PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein is abnormally distributed and overexpressed. PBC enventually leads to cirrhosis and liver failure. Mutations in this gene are also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lactic acidosis in infancy and early childhood.[provided by RefSeq, Oct 2009]

Function:
The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). It contains multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3).

Subcellular Location:
Mitochondrion matrix.

DISEASE:
Note=Primary biliary cirrhosis is a chronic, progressive cholestatic liver disease characterized by the presence of antimitochondrial autoantibodies in patients' serum. It manifests with inflammatory obliteration of intra-hepatic bile duct, leading to liver cell damage and cirrhosis. Patients with primary biliary cirrhosis show autoantibodies against the E2 component of pyruvate dehydrogenase complex.
Defects in DLAT are the cause of pyruvate dehydrogenase E2 deficiency (PDHE2 deficiency) [MIM:245348]; also known as lactic acidemia due to defect of E2 lipoyl transacetylase of the pyruvate dehydrogenase complex. Pyruvate dehydrogenase (PDH) deficiency is a major cause of primary lactic acidosis and neurological dysfunction in infancy and early childhood. In this form of PDH deficiency episodic dystonia is the major neurological manifestation, with other more common features of pyruvate dehydrogenase deficiency, such as hypotonia and ataxia, being less prominent.

Similarity:
Belongs to the 2-oxoacid dehydrogenase family.
Contains 2 lipoyl-binding domains.

SWISS:
P10515

Gene ID:
1737

Database links:

Entrez Gene: 512723 Cow

Entrez Gene: 1737 Human

Entrez Gene: 235339 Mouse

Entrez Gene: 397054 Pig

Entrez Gene: 81654 Rat

Entrez Gene: 324201 Zebrafish

Omim: 608770 Human

SwissProt: P11180 Cow

SwissProt: P10515 Human

SwissProt: Q8BMF4 Mouse

SwissProt: P08461 Rat

Unigene: 335551 Human

Unigene: 285076 Mouse

Unigene: 471144 Mouse

Unigene: 15413 Rat



產(chǎn)品圖片
Sample: Lane 1: Mouse Cerebrum tissue lysates Lane 2: Mouse Heart tissue lysates Lane 3: Mouse Muscle tissue lysates Lane 4: Rat Cerebrum tissue lysates Lane 5: Rat Muscle tissue lysates Lane 6: Human PANC-1 cell lysates Primary: Anti-PDCE2 (bs-19695R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 63 kDa Observed band size: 63 kDa
Paraformaldehyde-fixed, paraffin embedded (rat stomach tissue); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (PDCE2) Polyclonal Antibody, Unconjugated (bs-19695R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
版權(quán)所有 2004-2026 m.nmgps.com 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書(shū)編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書(shū)編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
日本三级视频在线观看 | 亚洲国产无码AV三区 | 波多野结衣被肉翻猛高潮 | 深夜催精毛片久久久久久 | 一个舔一个插视频免费 | 亚洲无码视频在线观看 | A片视频免费在线播放 | 肉色丝袜玉足诱惑自慰在线免费观看 | 四州少妇BBw搡BBBB | 日韩视频在线观看免费 | 亚洲AV成人无码精品区 | 超碰96极品1区| 成人精品视频99在线观看免费 | 少妇无码无套AV一区 | 亚洲精品国产手机 | 成人 精品美女隐私漫画 | 嫖妓老熟女嗷嗷叫91在线 | 美女裸体网站熟女一区 | 18 无套直国产 | 熟女 人妻蜜臀AⅤ青椒 | 91精品一区二区在线观看 | 国产一级a毛一级a看免费视频乱 | 国产成人精品 水 国产成人精品AA毛片 | 久久久国产精品人人片 | 四川少妇A片免费观看 | 三亚三黄三色AAA毛片 | av免费在线观看网站 | 呦小BBw搡BBBB一线天 | 搡六十70老女人老熟女视频 | 日韩女女同性AA女同 | 91亚洲精品国偷拍自产在线观看 | 四川BBB搡BBB搡多 | 亚洲第三区无码17c 黄色三级国产色情无码 | 东北少妇监控在线播放 | 国产熟妇婬乱A片免费看牛牛 | 特级丰满少妇一级AAAA爱毛片,17 | 亂倫近親相姦中文字幕网站 | 成人国产AV一级毛片无码 | 思思99re6国产精品视频 | 亚洲AV不卡无毒免费在线 | 中文字幕巨乱亚洲高清A片28 |