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)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(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
特级西西444www大胆高清图片,免费无套内谢少妇毛片A片软三
首頁(yè) > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
ALAS-E Rabbit pAb (bs-9516R)  
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/詢價(jià)

產(chǎn)品編號(hào) bs-9516R
英文名稱 ALAS-E Rabbit pAb
中文名稱 5-氨基乙酰丙酸合酶1抗體
別    名 5-aminolevulinate synthase, erythroid-specific, mitochondrial; 5-aminolevulinic acid synthase; ALAS E; ALASE; ANH1; delta aminolevulinate synthase; XLSA; 5 aminolevulinic acid synthase 2; 5-aminolevulinate synthase 2; 5-aminolevulinate synthase; 5-aminole  
研究領(lǐng)域 腫瘤  心血管  細(xì)胞生物  免疫學(xué)  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human (predicted: Mouse,Rat,Rabbit,Pig,Sheep,Cow,Dog,Horse)
產(chǎn)品應(yīng)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 59 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ALAS2/ALAS-E: 101-200/587 
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 5-aminolevulinate synthase 1 (ALAS-H) and 2 (ALAS-E) are two isoforms of ALAS, an enzyme catalyzing the first step of the heme biosynthetic pathway in mammals. The erythroid-specific isoenzyme, ALAS-E, regulates the first step of hematopoietic cell differentation and iron metabolism in the liver. ALAS-H is a housekeeping protein which mediates synthesis of early heme in the mitochondria of most cells. Succinyl CoA associates with ALAS-E in protein conformation change and translocation of ALAS-E into the mitochondria and does not interact with ALAS-H. The ALAS-E 5'-flanking region contains binding sites for nuclear activators such as GATA-1, NF-E2 and EKLF. Since the ALAS gene maps to the X chromosome, mutation of the gene leads to the pyridoxine-refractory X-linked sideroblastic anemia.

Subunit:
Homodimer. Interacts with SUCLA2.

Subcellular Location:
Mitochondrion matrix

Tissue Specificity:
Erythroid specific.

DISEASE:
Defects in ALAS2 are a cause of anemia sideroblastic X-linked (XLSA) [MIM:300751]. Sideroblastic anemia is characterized by anemia of varying severity, hypochromic peripheral erythrocytes, systemic iron overload secondary to chronic ineffective erythropoiesis, and the presence of bone marrow ringed sideroblasts. Sideroblasts are characterized by iron-loaded mitochondria clustered around the nucleus. XLSA shows a variable hematologic response to pharmacologic doses of pyridoxine.
Defects in ALAS2 are the cause of erythropoietic protoporphyria X-linked dominant (XLDPT) [MIM:300752]. Porphyrias are inherited defects in the biosynthesis of heme, resulting in the accumulation and increased excretion of porphyrins or porphyrin precursors. They are classified as erythropoietic or hepatic, depending on whether the enzyme deficiency occurs in red blood cells or in the liver. XLDPT is a form of porphyria characterized biochemically by a high proportion of zinc-protoporphyrin in erythrocytes, in which a mismatch between protoporphyrin production and the heme requirement of differentiating erythroid cells leads to overproduction of protoporphyrin in amounts sufficient to cause photosensitivity and liver disease. Note=Gain of function mutations in ALS2 are responsible for XLDPT, but they can also be a possible aggravating factor in congenital erythropoietic porphyria and other erythropoietic disorders caused by mutations in other genes (PubMed:21309041).

Similarity:
Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family.

SWISS:
P22557

Gene ID:
212

Database links:

Entrez Gene: 212 Human

Entrez Gene: 11656 Mouse

Entrez Gene: 25748 Rat

Omim: 301300 Human

SwissProt: P22557 Human

SwissProt: P08680 Mouse

SwissProt: Q63147 Rat

Unigene: 522666 Human

Unigene: 555936 Human

Unigene: 302724 Mouse

Unigene: 226279 Rat

Unigene: 32517 Rat



產(chǎn)品圖片
Sample: Lane 1: Human MOLT4 cell lysates Lane 2: Human K562 cell lysates Primary: Anti-ALAS-E (bs-9516R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 59 kDa Observed band size: 62 kDa
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    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
天天躁日日躁aaaaxxxx欧美 | 黄片视频在线观看免费 | 91精品久久久久久久 | 中文字幕aV无码一区二区三区 | 边添小泬边狠狠躁视频 | 日本韩国成人网站 | 亚洲精品成人a v无码A片午夜 | 丝袜美腿中文 影音先锋 | 黄色在线免费观看视频 | 特一妇一性一视一频 | 久久久亚洲中文字幕 | 免费一级婬片AA片观看 | 91精品国产综合久久久果冻传媒 | 国产伦精品一区二区三区视频女 | 五十路熟妇亚洲AV无码 | 日本丰满无码一区久久 | 精品国产美女裸身无遮挡AV上网站 | 91爱豆传媒国产成人网站 | 美女露逼黄色视频网站免费看 | 欧美精品久久久久久久久爆乳 | 蜜桃视频在线观看免费 | 国产精品扒开腿做爽爽 | 亂倫近親相姦免费中文字幕 | 成人精品一区二区三区A片用毒蛇 | 性感丰满爆乳少妇无码中出福利视频 | 蜜桃视频com.www | 91熟妇女人妻69丰满少妇 | 红桃视频在线观看免费一区二区三区 | 亚洲精品一区久久久久久 | 特黄A片久久人妻少妇 | 国产精品久久久久亚洲AV | 国产三级一区二区三区在线观看 | 西西人体444WWW无码男男 | 囯产伦精一区二区三区妓 | 潘金莲一级XxX片 | 波多野结衣人妻无码8mv | 亚洲国产精品无码久久小说 | 精品一区二区三区视频 | 亚洲6080yy久久无码产自国产· | 精品久久BBBBB精品人妻 | 精品 码产区一区二区三区 麻豆国产一区二区三区四区 |