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RabbitAnti-BTR1 Rabbit pAb  antibody (bs-22390R)
~~~促销,代码KXJ230206~~~
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价

产品编号 bs-22390R
英文名称 BTR1 Rabbit pAb
中文名称 钙粘蛋白相关蛋白受体BTR1抗体
别    名 BTR1; CDPD1; CHED; CHED2; NABC1; dJ794I6.2; S4A11_HUMAN; SLC4A11; Sodium borate cotransporter 1 (NaBC1); S4A11_MOUSE;   
研究领域 细胞生物  免疫学  信号转导  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 Human,  (predicted: Mouse, Rat, )
产品应用 WB=1:500-2000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 100 kDa
检测分子量 92
细胞定位 细胞膜 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human BTR1 : 61-160/891 <Cytoplasmic>
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 BtR1 is a cadherin receptor from the tobacco hornworm Manduca sexta.

Function:
Transporter which plays an important role in sodium-mediated fluid transport in different organs. Prevents severe morphological changes of the cornea caused by increased sodium chloride concentrations in the stroma. In the inner ear, is involved in transport of potassium through the fibrocyte layer to the stria vascularis and is essential for the generation of the endocochlear potential but not for regulation of potassium concentrations in the endolymph. In the kidney, is essential for urinary concentration, mediates a sodium flux into the thin descending limb of Henle loop to allow countercurrent multiplication by osmotic equilibration (By similarity). Involved in borate homeostasis. In the absence of borate, it functions as a Na(+) and OH(-)(H(+)) channel. In the presence of borate functions as an electrogenic Na(+) coupled borate cotransporter.

Subunit:
Homodimer.

Subcellular Location:
Cell membrane. Membrane; Multi-pass membrane protein.

Tissue Specificity:
Widely expressed. Highly expressed in kidney, testis, salivary gland, thyroid, trachea and corneal endothelium. Not detected in retina and lymphocytes.

Post-translational modifications:
Glycosylated.

DISEASE:
Corneal dystrophy and perceptive deafness (CDPD) [MIM:217400]: An ocular disease characterized by the association of corneal clouding with progressive perceptive hearing loss. Note=The disease is caused by mutations affecting the gene represented in this entry.
Corneal dystrophy, endothelial 2, autosomal recessive (CHED2) [MIM:217700]: A congenital corneal dystrophy characterized by thickening and opacification of the cornea, altered morphology of the endothelium, and secretion of an abnormal collagenous layer at the Descemet membrane. Note=The disease is caused by mutations affecting the gene represented in this entry.
Corneal dystrophy, Fuchs endothelial, 4 (FECD4) [MIM:613268]: A corneal disease caused by loss of endothelium of the central cornea. It is characterized by focal wart-like guttata that arise from Descemet membrane and develop in the central cornea, epithelial blisters, reduced vision and pain. Descemet membrane is thickened by abnormal collagenous deposition. Note=The disease is caused by mutations affecting the gene represented in this entry.

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

SWISS:
Q8NBS3

Gene ID:
83959

Database links:

Entrez Gene: 83959 Human

Entrez Gene: 532407 Cow

Entrez Gene: 269356 Mouse

Entrez Gene: 311423 Rat

Omim: 610206 Human

SwissProt: Q8NBS3 Human

SwissProt: A2AJN7 Mouse

Unigene: 105607 Human

Unigene: 441391 Mouse



产品图片
Sample: HepG2 (Human) Cell Lysate at 30 ug A549 (Human) Cell Lysate at 30 ug U2os (Human) Cell Lysate at 30 ug MCF-7 (Human) Cell Lysate at 30 ug Primary: Anti-BTR1 (bs-22390R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 90 kD Observed band size: 92 kD
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