麻豆av资源_日本三级一区_www.狠狠艹_国产精妇在线观看第一区_成人性生交大片免费看中国A片_日本一本久久

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
久久亚洲色WWW成人,一本久久精品一区二区,人人99精
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-SLC4A4/PE Conjugated antibody (bs-2096R-PE)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-2096R-PE
英文名稱 Rabbit Anti-SLC4A4/PE Conjugated antibody
中文名稱 PE標記的碳酸氫鈉協同轉運蛋白4-A4抗體
別    名 DKFZp781H1314; Electrogenic sodium bicarbonate cotransporter 1; hhNMC; HNBC 1; HNBC1; kNBC 1; KNBC; kNBC1; Na(+)/HCO3(-) cotransporter; Na+HCO3- cotransporter 4; NBC 1; NBC 2; NBC1; NBC2; Nbc4; NBCE 1; NBCE1; PNBC; SLC4A5; Sodium bicarbonate cotransporter kidney; sodium bicarbonate cotransporter member 4; Sodium bicarbonate cotransporter pancreas; Solute carrier family 4 member 4; solute carrier family 4 sodium bicarbonate cotransporter member 4; Solute carrier family 4 sodium bicarbonate cotransporter member 5.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 通道蛋白  轉運蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Rabbit, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 116kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human electrogenic sodium bicarbonate cotransporter 1 isoform 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.
產品介紹 background:
SLC4A4 (Electrogenic sodium bicarbonate cotransporter 1) is an electrogenic sodium/bicarbonate cotransporter with a Na(+):HCO3(-) stoichiometry varying from 1:2 to 1:3. It may regulate bicarbonate influx/efflux at the basolateral membrane of cells and regulate intracellular pH. SLC4A4 interacts with carbonic anhydrase 2 and carbonic anhydrase 4 which may regulate transporter activity. There are four named isoforms produced by alternative splicing.

This gene encodes a sodium bicarbonate cotransporter (NBC) involved in the regulation of bicarbonate secretion and absorption and intracellular pH. Mutations in this gene are associated with proximal renal tubular acidosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008].

Function:
Electrogenic sodium/bicarbonate cotransporter with a Na(+):HCO3(-) stoichiometry varying from 1:2 to 1:3. May regulate bicarbonate influx/efflux at the basolateral membrane of cells and regulate intracellular pH.

Subunit:
Interacts with CA2/carbonic anhydrase 2 and CA4/carbonic anhydrase 4 which may regulate transporter activity.

Subcellular Location:
Basolateral cell membrane; Multi-pass membrane protein.

Tissue Specificity:
Isoform 1 is expressed in pancreas and to a lower extent in heart, skeletal muscle, liver, parotid salivary glands, prostate, colon, stomach, thyroid, brain and spinal chord. Corneal endothelium cells express only isoform 1 (at protein level). Isoform 2 is specifically expressed in kidney at the level of proximal tubules.

Post-translational modifications:
Phosphorylation of Ser-1026 by PKA increases the binding of CA2 and changes the Na(+):HCO3(-) stoichiometry of the transporter from 3:1 to 2:1. Phosphorylation of Thr-49 regulates isoform 1 conductance.
N-glycosylation is not necessary for the transporter basic functions.

DISEASE:
Defects in SLC4A4 are the cause of proximal renal tubular acidosis with ocular abnormalities (pRTA-OA) [MIM:604278]; also known as renal tubular acidosis II. Caused by an impairment of bicarbonate absorption in the proximal tubule, proximal renal tubular acidosis (pRTA) is characterized by a decreased renal HCO3(-) threshold. pRTA-OA is an extremely rare autosomal recessive syndrome characterized by short stature, profound pRTA, mental retardation, bilateral glaucoma, cataracts and bandkeratopathy.
Note=Loss of interaction with and stimulation by CA4 is the cause of retinitis pigmentosa type 17 (RP17).

Similarity:
Belongs to the anion exchanger (TC 2.A.31) family.

Database links:

Entrez Gene: 8671 Human

Entrez Gene: 84484 Rat

Omim: 603345 Human

SwissProt: Q9Y6R1 Human

SwissProt: Q9XSZ4 Rabbit

SwissProt: Q9JI66 Rat

Unigene: 5462 Human

Unigene: 11114 Rat



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 m.jywcc.com 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: 欧美国产在线不卡 | 国产AV国片精品有毛 | 99久久99久久精品免费看 | 久久亚洲一区二区三区四区 | 国产一级毛片视频 | 欧美专区福利 | 超碰在线视97 | 欧美午夜片欧美片在线观看 | 欧美天堂久久 | 色5566| 国产亚洲日韩在线播放更多 | 毛片视频网站在线观看 | 性开放欧美瑜伽TV | av一区在线播放 | 91琪琪在线| 农村少妇无套内谢粗又长 | 波多野结衣在线视频免费观看 | 日韩女人一级 | 3344在线看片免费 | 亚洲精品久久久无码白峰美 | 亚洲免费激情 | 欧美一区二区三区四 | 日本深夜福利视频 | 国产区精品 | WWW亚洲色大成网络.COM | 黑鬼吊太大少妇尖叫 | 黑人40厘米全部进去A片 | 秋霞影视一区 | 国产伊人av | 96精品成人无码A片观看金桔 | 天堂资源中文WWW | 国产精品亚洲АV无码播放 毛片软件 | 成人深夜福利视频 | 欧美性XXXX丰满极品少妞 | 日韩美女啪啪 | 精品久久日本影视一区 | 福利在线看 | 香蕉丝瓜榴莲在线观看 | 国产黄色的视频 | 成在人线AV无码免费 | 国自产拍亚洲免费视频 |