吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

掃碼關(guān)注公眾號           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  人才招聘  關(guān)于我們  聯(lián)系我們
久久久久无码专区亚洲AV,男阳茎进女阳道视频大全
Rabbit Anti-COX3/PE Conjugated antibody (bs-3934R-PE)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號 bs-3934R-PE
英文名稱1 Rabbit Anti-COX3/PE Conjugated antibody
中文名稱 PE標(biāo)記的細(xì)胞色素C氧化酶亞基3抗體
別    名 Cytochrome c oxidase polypeptide III; Cytochrome c oxidase subunit 3; COIII; COX3; COX-3; COXIII; MT CO3; MTCO3; COX3_HUMAN; mitochondrially encoded cytochrome c oxidase III; MT-CO3.  
規(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 腫瘤  細(xì)胞生物  免疫學(xué)  神經(jīng)生物學(xué)  信號轉(zhuǎn)導(dǎo)  轉(zhuǎn)錄調(diào)節(jié)因子  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Mouse, Rat,  (predicted: Human, Chicken, Dog, Pig, Cow, Horse, Rabbit, )
產(chǎn)品應(yīng)用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 30kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human COX3
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(chǎn)品介紹 Function:
Subunits I, II and III form the functional core of the enzyme complex.

Subcellular Location:
Mitochondrion inner membrane; Multi-pass membrane protein.

DISEASE:
Leber hereditary optic neuropathy (LHON) [MIM:535000]: A maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction. Cardiac conduction defects and neurological defects have also been described in some patients. LHON results from primary mitochondrial DNA mutations affecting the respiratory chain complexes. Note=The disease is caused by mutations affecting the gene represented in this entry.
Mitochondrial complex IV deficiency (MT-C4D) [MIM:220110]: A disorder of the mitochondrial respiratory chain with heterogeneous clinical manifestations, ranging from isolated myopathy to severe multisystem disease affecting several tissues and organs. Features include hypertrophic cardiomyopathy, hepatomegaly and liver dysfunction, hypotonia, muscle weakness, exercise intolerance, developmental delay, delayed motor development and mental retardation. Some affected individuals manifest a fatal hypertrophic cardiomyopathy resulting in neonatal death. A subset of patients manifest Leigh syndrome. Note=The disease is caused by mutations affecting the gene represented in this entry.
Recurrent myoglobinuria mitochondrial (RM-MT) [MIM:550500]: Recurrent myoglobinuria is characterized by recurrent attacks of rhabdomyolysis (necrosis or disintegration of skeletal muscle) associated with muscle pain and weakness, and followed by excretion of myoglobin in the urine. Note=The gene represented in this entry may be involved in disease pathogenesis.

Similarity:
Belongs to the cytochrome c oxidase subunit 3 family.

Database links:

Entrez Gene: 281921 Cow

Entrez Gene: 4514 Human

Entrez Gene: 17710 Mouse

Entrez Gene: 26204 Rat

Omim: 516050 Human

SwissProt: P00415 Cow

SwissProt: P00414 Human

SwissProt: P00416 Mouse

SwissProt: P05505 Rat




Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.xucheq.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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(wǎng)安備110107000727號
男人吃奶摸下挵进去啪啪软件| 欧美人与动性XXXXX杂性| 蜜臀AV在线播放一区二区三区| 久久久国产一区二区三区四区小说| 亚洲色偷偷综合亚洲AV78| 国产精品无码V在线观看| 国产精品久久久久一区二区三区| 无码88AⅤ欧美熟妇人妻影院| 亚洲精品无码永久中文字幕| 肥嫩多毛的大荫户| 欧美乱大交XXXXX潮喷| 免费的视频APP网站| 国产深夜男女无套内射| 公交车被cao到合不拢腿 | 又大又长粗又爽又黄少妇视频| 欧美精品视频| 女人被强╳到高潮喷水在线观看| 蜜臀AV无码精品人妻色欲| 中文字幕精品久久久久人妻| 日日碰狠狠添天天爽无码| 色噜噜狠狠色综合久夜色撩人| 亚洲精品国产成人| 欧美午夜理伦三级在线观看| 精品欧美А∨无码黑人| 日韩AV高清无码| 特黄A级毛片| 亚洲AV成人片无码| 亂倫近親相姦中文字幕| 国产精品久久久久久久久免费| 不许人间见白头| 夜夜添无码一区二区三区| 日韩AV无码一区二区三区不卡| AV网站在线观看| 日韩人妻无码一区二区三区| 暴力调教一区二区三区 | 射精视频| 亚洲乱码日产精品BD在线观看| 国产又色又爽又高潮免费| 中文字幕精品av乱码在线| 香蕉久久一区二区不卡无毒影院| 最近2019中文字幕大全第二页|