超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

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  關(guān)于我們  聯(lián)系我們
在线免费观看福利,日韩一卡2卡3卡4卡2021免费观看国色天香 ,男女啪啪免费体验区
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-FLJ11506/Biotin Conjugated antibody (bs-16102R-Bio)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-16102R-Bio
英文名稱 Rabbit Anti-FLJ11506/Biotin Conjugated antibody
中文名稱 生物素標記的AAGAB蛋白抗體
別    名 AAGAB; AAGAB_HUMAN; Alpha and gamma adaptin binding protein p34; Alpha- and gamma-adaptin-binding protein p34; LOC79719;   
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 細胞生物  信號轉(zhuǎn)導(dǎo)  轉(zhuǎn)運蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Rat,  (predicted: Human, Mouse, Dog, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應(yīng)用 WB=1:50-200 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 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 35kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FLJ11506
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 background:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FLJ11506 gene product has been provisionally designated FLJ11506 pending further characterization.

Function:
May play a role in membrane traffic.

Subunit:
Associated with AP-1 and AP-2 complexes.

Subcellular Location:
Cytoplasm, cytosol.

Tissue Specificity:
Widely expressed, including in skin and keratinocytes, with highest levels in adrenal gland, rectum and thymus.

DISEASE:
Keratoderma, palmoplantar, punctate 1A (PPKP1A) [MIM:148600]: An autosomal dominant dermatological disorder characterized by multiple hyperkeratotic, centrally indented, papules that develop in early adolescence, or later, and are irregularly distributed on the palms and soles (other palmoplantar keratoses have mostly diffuse hyperkeratinization). In mechanically irritated areas, confluent plaques can be found. Interfamilial and intrafamilial severity shows broad variation. In some cases, PPKP1 is associated with the development of early- and late-onset malignancies, including squamous cell carcinoma. Note=The disease is caused by mutations affecting the gene represented in this entry.

Database links:

Entrez Gene: 79712 Human

Entrez Gene: 79719 Human

Entrez Gene: 171435 Rat

Omim: 614888 Human

SwissProt: Q4AE62 Human

SwissProt: Q6PD74 Human

SwissProt: Q9R0Z7 Rat

Unigene: 254642 Human

Unigene: 163023 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.ggggww.cn 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
主站蜘蛛池模板: 精品无人区麻豆乱码无限制 | 性少妇xxxxx 精品视频一二三 | 人妻日本无中文字幕无码 | 久久精品国产亚洲7777 | 日本熟妇HDSEX视频 | 亚洲国产中文字幕新在线vr | 亚洲精品18日本一区久久 | 亚洲综合无码一区二区加勒此 | 久久不见久久见免费影院视频观看 | 国产69精品久久久久按摩 | 麻豆1区 | 亚洲日韩成人无码私人影院 | 密色影院 | 国产精品久久久久永久免费 | 欧美怕怕视频 | 天堂在线中文 | 99香蕉国产精品偷在线观看 | 狠狠干天天射 | 欧美一区二区在线视频 | 激情内射亚洲一区二区三区爱妻 | 亚洲av日韩av综合 | 区二区欧美性插b在线视频网站 | 国产成人A∨麻豆精品 | 日本视频网站在线观看 | 91天天操 | 亚洲无亚洲人成网站77777 | 99久久99久久精品国产片 | youjizz中国少妇 | 亚洲AV永久无码精品放毛片 | 一级黄色毛片播放 | 一级特黄大片色 | 一级国产片 | 久久天堂综合亚洲伊人hd妓女 | 亚洲综合激情五月丁香六月 | 在线看播放免费网站 | 亚洲日韩欧美一区二区三区 | 亚州中文字幕在线观看 | 超碰色在线 | 一区二区三区影视 | 国产精品综合AV一区二区国产馆 | 国产精品美女久久久av超清 |