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  人才招聘  關于我們  聯(lián)系我們
无码专区国产精品一区,久久综合亚洲欧美区
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-NIPA-2/BF647 Conjugated antibody (bs-7465R-BF647)
訂購熱線:400-901-9800
訂購郵箱:sales@www.p2b3.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.p2b3.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-7465R-BF647
英文名稱1 Rabbit Anti-NIPA-2/BF647 Conjugated antibody
中文名稱 BF647標記的鎂轉運蛋白NIPA2抗體
別    名 Magnesium transporter NIPA2; MGC5466; NIPA 2; NIPA2_HUMAN; NIPA2; Non imprinted in Prader Willi/Angelman syndrome 2; Non imprinted in Prader Willi/Angelman syndrome region protein 2.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  免疫學  信號轉導  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, Chicken, Dog, Cow, Rabbit, )
產(chǎn)品應用 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 36kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human NIPA-2
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:
This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]

Function:
This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Widely expressed.

Similarity:
Belongs to the NIPA family.

Database links:

Entrez Gene: 81614 Human

Entrez Gene: 507430 Cow

Entrez Gene: 479002 Dog

Entrez Gene: 93790 Mouse

Omim: 608146 Human

SwissProt: Q3SWXO Cow

SwissProt: Q8N8Q9 Human

SwissProt: Q9JJC8 Mouse

Unigene: 591003 Human



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.p2b3.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(yī)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(wǎng)安備110107000727號
宜君县| 芒康县| 登封市| 惠水县| 丹东市| 河曲县| 平武县| 拜泉县| 汉阴县| 莆田市| 甘南县| 蕲春县| 东港市| 济阳县| 瓦房店市| 兴城市| 石台县| 阿巴嘎旗| 法库县| 甘谷县| 毕节市| 朔州市| 昌黎县| 林甸县| 馆陶县| 牡丹江市| 望都县| 柳林县| 青浦区| 大石桥市| 伊金霍洛旗| 临澧县| 岳阳市| 榕江县| 长汀县| 藁城市| 兴化市| 定边县| 伊宁县| 昭苏县| 永年县|