mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

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  人才招聘  關(guān)于我們  聯(lián)系我們
日本视频一区二区二三区,国产熟女婷婷免费视频,亚洲欧美专区一区二区
Rabbit Anti-phospho-PLB (Thr17)/PE Conjugated antibody (bs-7483R-PE)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@m.p2b3.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@m.p2b3.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-7483R-PE
英文名稱1 Rabbit Anti-phospho-PLB (Thr17)/PE Conjugated antibody
中文名稱 PE標(biāo)記的磷酸化心臟磷蛋白抗體
別    名 Phospholamban (phospho T17); p-Phospholamban (T17); Phospho-Phospholamban (Thr17); phospholamban(phospho Thr17); p-PLB(T17); Cardiac phospholamban; CMD1P; PLB; PLN; PPLA_HUMAN.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說 明 書 100ul  
產(chǎn)品類型 磷酸化抗體 
研究領(lǐng)域 心血管  細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應(yīng)用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 6kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human phospho-PLB (Thr17)
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 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 background:
The protein encoded by this gene is found as a pentamer and is a major substrate for the cAMP-dependent protein kinase in cardiac muscle. The encoded protein is an inhibitor of cardiac muscle sarcoplasmic reticulum Ca(2+)-ATPase in the unphosphorylated state, but inhibition is relieved upon phosphorylation of the protein. The subsequent activation of the Ca(2+) pump leads to enhanced muscle relaxation rates, thereby contributing to the inotropic response elicited in heart by beta-agonists. The encoded protein is a key regulator of cardiac diastolic function. Mutations in this gene are a cause of inherited human dilated cardiomyopathy with refractory congestive heart failure. [provided by RefSeq, Jul 2008].

Function:
Phospholamban has been postulated to regulate the activity of the calcium pump of cardiac sarcoplasmic reticulum

Subcellular Location:
Mitochondrion membrane. Sarcoplasmic reticulum.

Tissue Specificity:
Heart.

Post-translational modifications:
Phosphorylated at Thr-17 by CaMK2, and in response to beta-adrenergic stimulation. Phosphorylation by DMPK may stimulate sarcoplasmic reticulum calcium uptake in cardiomyocytes.

DISEASE:
Defects in PLN are the cause of cardiomyopathy dilated type 1P (CMD1P) [MIM:609909]. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Defects in PLN are the cause of cardiomyopathy familial hypertrophic type 18 (CMH18) [MIM:613874]. CMH18 is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.

Similarity:
Belongs to the phospholamban family.

Database links:

Entrez Gene: 5350 Human

Entrez Gene: 18821 Mouse

Entrez Gene: 64672 Rat

Omim: 172405 Human

SwissProt: P26678 Human

SwissProt: P61014 Mouse

SwissProt: P61016 Rat

Unigene: 170839 Human

Unigene: 34145 Mouse

Unigene: 9740 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.m.p2b3.cn 北京博奧森生物技術(shù)有限公司
通過國(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)
中文字幕一区二区三区免费看| 国产婷婷av一区二区| 国产一级二级三级精品| 久久中文字幕一区不卡| 国产A级三级三级三级视频| 亚洲mm视频网站在线播放| 99国产精品视频在线| 国产性生活视频免费| 日本成人免费一区二区三区| 欧美日韩一级片在线| 久久婷婷综合激情亚洲狠狠| 国产精品久久小视频| 国产一二三区亚洲欧美| 花花草草寻亲记哪里看全集| 亚洲av成人精品日韩一区麻豆| 精品久久久久久久久久中文幕| 极品少妇欧美一区二区| 日本视频免费一区二区| 日韩在线中文字幕观看| 夫妇交换性4中文字幕无码| 欧美成人伦理在线播放| 精品一区二区三区日韩| 亚洲精品日韩在线丰满| 人妻精品人妻一区区| 中文亚洲欧美日韩国产| 亚洲精品一区二区三区中文字幕| 日产国产精品久久久久久| 欧美日韩永久精品一区二区| 日韩一区二区人妻9999| 中文字幕无码aⅴ免费不卡| 95精品视频在线观看| 中文字幕字幕一区二区三区| 韩国爱情电影年轻的母亲| 亚洲精品在线观看日本国产| 日本日本乱码伦视频免费| 亚洲精品夜夜夜妓女网| 亚洲中文字幕在线视频一区| 亚洲av成人精品日韩一区麻豆| 中文字幕人妻乱一区二区三区| 久久久久久久久久久极品| 国产盗摄精品一区二区视频|