亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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  聯系我們
日本成人免费在线视频,日本xxxx裸体xxxx,99精品无人区乱码1区2区3区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-mucolipin 1/HRP Conjugated antibody (bs-18731R-HRP)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-18731R-HRP
英文名稱 Rabbit Anti-mucolipin 1/HRP Conjugated antibody
中文名稱 辣根過氧化物酶標記的粘脂蛋白1抗體
別    名 MCLN1_HUMAN ; Mcoln 1 ; Mcoln1 ; MG 2 ; MG-2 ; MG2 ; ML 4 ; ML4 ; MLIV ; MST080 ; MSTP080 ; Mucolipidin ; Mucolipin-1 ; Mucolipin1 ; TRP ML1 ; TRPML1.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  免疫學  信號轉導  跨膜蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Pig, Cow, Rabbit, Sheep, Monkey, Cat, )
產品應用 WB=1:500-2000 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 65kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human mucolipin 1
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.
產品介紹 background:
This gene encodes a memberof the transient receptor potential (TRP) cation channel gene family. The transmembrane protein localizes to intracellular vesicular membranes including lysosomes, and functions in the late endocytic pathway and in the regulation of lysosomal exocytosis. The channel is permeable to Ca(2+), Fe(2+), Na(+), K(+), and H(+), and is modulated by changes in Ca(2+) concentration. Mutations in this gene result in mucolipidosis type IV. [provided by RefSeq, Oct 2009]

Function:
Cation channel probably playing a role in the endocytic pathway and in the control of membrane trafficking of proteins and lipids. Could play a major role in Ca(2+) transport regulating lysosomal exocytosis.

Subcellular Location:
Cell membrane. Late endosome membrane. Lysosome membrane.Entrez Gene: 57192 Human Entrez Gene: 94178 Mouse Entrez Gene: 288371 Rat Omim: 605248 Human SwissProt: Q9GZU1 Human SwissProt: Q99J21 Mouse Unigene: 567548 Human Unigene: 631858 Human Unigene: 8356 Mouse

Tissue Specificity:
Widely expressed in adult and fetal tissues.

DISEASE:
Defects in MCOLN1 are the cause of mucolipidosis type IV (MLIV) [MIM:252650]; also known as sialolipidosis. MLIV is an autosomal recessive lysosomal storage disorder characterized by severe psychomotor retardation and ophthalmologic abnormalities, including corneal opacity, retinal degeneration and strabismus. Storage bodies of lipids and water-soluble substances are seen by electron microscopy in almost every cell type of the patients. Most patients are unable to speak or walk independently and reach a maximal developmental level of 1-2 years. All patients have constitutive achlorhydia associated with a secondary elevation of serum gastrin levels. MLIV may be due to a defect in sorting and/or transport along the late endocytic pathway. MLIV is found at relatively high frequency among Ashkenazi Jews.

Similarity:
Belongs to the transient receptor (TC 1.A.4) family. Polycystin subfamily. MCOLN1 sub-subfamily.

Database links:

Entrez Gene: 57192 Human

Entrez Gene: 94178 Mouse

Entrez Gene: 288371 Rat

Omim: 605248 Human

SwissProt: Q9GZU1 Human

SwissProt: Q99J21 Mouse

Unigene: 567548 Human

Unigene: 631858 Human

Unigene: 8356 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.www.chomd.com.cn 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
主站蜘蛛池模板: 久久精品免费一区二区三区y| 国产成人精品三级在线观看_| 又黑又重又大又圆| 中文字幕综合亚洲jav| 久久精品动漫一区二区三区男男动画片| 久久精品国产久精国产|亚洲日韩中文第一精品| 精品久久久久久久无码雪峰影视| 草莓视频在线观看国产剧情| 亚洲精品高清国产久久久久久| 久久精品国产99精品国产202|亚洲| 91精品国产91久久久久久一区二区| 四虎浮力视频在线播放| 国产露出调教福利91| 亚洲精品中文字幕乱码无线中文字幕亚洲 | 国产自啪精品视频网站丝袜玉足| 竹菊视频在线观看高清免费播放| 少妇邻居内射在线,内射口| 动漫精品一区二区三区av| 小荡货又粗又长又硬又爽A片图片| 精品久久亚洲中文无码字幕| 艳妇乳欲伦岳| 国产自啪精品视频网站丝袜玉足| 亚洲中文综合无码字幕在线观看| 久久精品人成免费一区二区三区| 又色又爽又黄的视频网站_欧美顶级牲交片_| 男人的天堂一区二区三区日韩| 1204人成网站色www| 久久人妻少妇嫩草AV蜜桃_久久久久亚洲AV成人无码 | 中文字幕免费视频一二三四 | 艳妇乳欲伦岳| 国产又爽又黄无码无遮挡风月| 亚洲美女又黄又爽在线观看穿越 | 日韩超碰人人爽人人做人人添_ | 日韩一区二区三区免费播放国| 99久久综合精品国产首员无码男同 | 非洲无码AAA视频| 美腿丝袜一区二区三区诱惑| 中国美女一级看片40分钟视频| 狠狠躁天天躁无码中文字幕按摩师| 亚洲精品无码人妻无码专区 | 国产综合一区二区在线观看户外导航 |