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(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 rvdoil.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)
国产伦子伦露脸免费视频 | 国产又大又粗又黄的视频 | caoporon| 六十路老熟女亂伦 | 又黄又粗又大在线播 | 久久国产精品人妻aⅴ | 91色屁屁TS人妖系列二区 | 国产 高潮 喷水 白浆 黑人 | 夜夜嗨中文无码视频 | 国产激情久久久久久一级A片老师 | 久久精品毛品无码一区三区 | 一级91毛片特大毛片 | 亚洲精品久久久久毛片A级桃花岛 | 国产伦精品一区二区三区88AV | 国产精品内射婷婷一级二 | 特级做a爰片毛片A片下载老人 | 国产无遮挡无黄又爽农村妇女 | 海南妇搡BBBB搡BBBB小说 | 亚洲精品无线乱码一区 | 91 黑料 精品 国产 | 国产精品十八禁一区二区 | 看黄色一级免费的黄色视频 | 亚洲黄片无码在线观看 | 色欲久久久天天天综合网 | 亚洲福利视频首页 | 小黄书成人版免费入口网站 | 亚洲第一页在线观看 | 亚洲精品色情婷婷在线播放 | 91睡熟迷奷系列精品 | 日本美女一级在线观看网站 | 免费中文字幕在线 | 搡60岁老女人老太婆免费 | 国产人妻一区二区三区欧美毛片 | 玩爽少妇性妇科一区二区 | 日本有码性爱视频在线一区 | 明里 无码一区二区三区 | 18禁无码毛片精品久久久久久 | 男女av免费观看高清 | 亚洲AV无码久久蜜桃杨思敏 | 你懂的欧日美一二 | 黄色网址视频观看大全 |