91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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(lián)系我們
日本无码一区二区三三,午夜国产精品秘 入口无码
首頁 > 產品中心 > 一抗 > 產品信息
phospho-PDHA1 (Ser293) Rabbit pAb (bs-4036R)  
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
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價

產品編號 bs-4036R
英文名稱 phospho-PDHA1 (Ser293) Rabbit pAb
中文名稱 磷酸化丙酮酸脫氫酶α1抗體
別    名 PDHA1(phospho Ser293); PDHA1(phospho S293); mitochondrial; somatic form; ODPA_HUMAN; PDH; PDHA1; PDHCE1A; PDHE1 A type I; PDHE1-A type I; PHE1A; Pyruvate Dehydrogenase(lipoamide) alpha 1; Pyruvate Dehydrogenase E1 alpha; Pyruvate dehydrogenase E1 component subunit alpha; Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial.  
產品類型 磷酸化抗體 
研究領域 腫瘤  細胞生物  免疫學  轉錄調節(jié)因子  激酶和磷酸酶  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse,Rat (predicted: Human,Rabbit,Pig,Cow,Chicken,Dog,Horse)
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 40 kDa
檢測分子量
細胞定位 細胞漿 線粒體
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated Synthesised phosphopeptide derived from human PDHA1 around the phosphorylation site of Ser293: GH(p-S)MS 
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 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 The pyruvate dehydrogenase (PDH) complex is a nuclear-encoded mitochondrial multienzyme complex that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle. The PDH complex is composed of multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase(E3). The E1 enzyme is a heterotetramer of two alpha and two beta subunits. This gene encodes the E1 alpha 1 subunit containing the E1 active site, and plays a key role in the function of the PDH complex. Mutations in this gene are associated with pyruvate dehydrogenase E1-alpha deficiency and X-linked Leigh syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Function:
The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and thereby links the glycolytic pathway to the tricarboxylic cycle.

Subunit:
Tetramer of 2 alpha and 2 beta subunits.

Subcellular Location:
Mitochondrion matrix.

Tissue Specificity:
Testis. Expressed in postmeiotic spermatogenic cells.

Post-translational modifications:
Phosphorylation at Ser-232, Ser-293 and Ser-300 by PDK family kinases inactivates the enzyme; for this phosphorylation at a single site is sufficient. Dephosphorylation at all three sites, i.e. at Ser-232, Ser-293 and Ser-300, is required for reactivation.

DISEASE:
Pyruvate dehydrogenase E1-alpha deficiency (PDHAD) [MIM:312170]: An enzymatic defect causing primary lactic acidosis in children. It is associated with a broad clinical spectrum ranging from fatal lactic acidosis in the newborn to chronic neurologic dysfunction with structural abnormalities in the central nervous system without systemic acidosis. Note=The disease is caused by mutations affecting the gene represented in this entry.
X-linked Leigh syndrome (X-LS) [MIM:308930]: Early-onset progressive neurodegenerative disorder with a characteristic neuropathology consisting of focal, bilateral lesions in one or more areas of the central nervous system, including the brainstem, thalamus, basal ganglia, cerebellum, and spinal cord. The lesions are areas of demyelination, gliosis, necrosis, spongiosis, or capillary proliferation. Clinical symptoms depend on which areas of the central nervous system are involved. The most common underlying cause is a defect in oxidative phosphorylation. LS may be a feature of a deficiency of any of the mitochondrial respiratory chain complexes. Note=The disease is caused by mutations affecting the gene represented in this entry.

SWISS:
P08559

Gene ID:
5160

Database links:

Entrez Gene: 5160 Human

Entrez Gene: 18597 Mouse

Entrez Gene: 29554 Rat

Omim: 300502 Human

SwissProt: A7MB35 Cow

SwissProt: P08559 Human

SwissProt: P35486 Mouse

SwissProt: P26284 Rat

Unigene: 530331 Human

Unigene: 34775 Mouse

Unigene: 3655 Rat



產品圖片
Sample: Lane 1: Mouse Cerebrum tissue lysates Lane 2: Mouse Muscle tissue lysates Lane 3: Mouse Heart tissue lysates Lane 4: Mouse Liver tissue lysates Lane 5: Rat Muscle tissue lysates Primary: Anti-phospho-PDHA1 (Ser293) (bs-4036R) at 1/1000 dilut
版權所有 2004-2026 www.rvdoil.com 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(yī)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
欧一美一交一交一乱一区二区三区 | 国产护士被 羞羞产奶一区二区 | 日本不卡视频在线观看 | 91蜜臀无码人妻久久精品 | 少妇搡BBBB搡BBB搡毛茸茸 | 91探花精品偷拍在线播放 | 好爽射深一点丰满视频 | 初尝黑人嗷嗷叫中文字幕91精品 | 国产精鲁鲁视频在线观看 | 亚洲91乱码毛片在线播放 | 婷婷欧美一区二区久久 | 欧美人妻在线视频video | eeuss鲁片一区二区三区四川 | 九九久久久久久亚洲精品 | 欧美日韩精品无码A片 | 国産精品久久久久久久 | ..少妇泬出白浆狠狠躁夜夜躁 | 中文字幕日韩一区 | 91亚洲精品久久久蜜桃 | 国产高清无码视频 | 亚洲国产成人在线 | 91人妻人人澡人人爽精品 | 精品國產亂子倫一區二區 | 波多野吉衣在线观看黄色 | 色狠狠色噜噜AV天堂五区消防 | 国偷自产视频一区二区久 | 国产一级婬片AAAAAA片麻代 | 红桃视频一区二区三区 | 免费看黄色视频的网站在线观看 | 成人午夜啪免费视频在线观看软件 | 扒丝袜午夜免费直播 | 男女无遮挡XX00动态图120秒 | 在线免费永久观看黄网站 | 国产亚洲视频在线观看 | 国产99视频在线观看 | 免费无码婬片AAAA片在线蜜芽 | 少妇高潮免费看一级A片出水图片 | 91黄色视频在线观看 | 91色屁屁TS人妖系列二区 | 国产成人无码视频 | 黄色视频里在线观看 |