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Rabbit Anti-KCNK9  antibody (bs-5933R)  
~~~促銷代碼KT202411~~~
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產(chǎn)品編號 bs-5933R
英文名稱 Rabbit Anti-KCNK9  antibody
中文名稱 TWIK相關(guān)酸敏感鉀離子通道蛋白9抗體
別    名 KCNK 9; KCNK-9; TASK3; Potassium channel subfamily K member 9; Acid-sensitive potassium channel protein TASK-3; TWIK-related acid-sensitive K(+) channel 3; Two pore potassium channel KT3.2; Short=Two pore K(+) channel KT3.2; KCNK9_HUMAN   
研究領(lǐng)域 腫瘤  免疫學  神經(jīng)生物學  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse,Rat (predicted: Human,Rabbit,Pig,Sheep,Cow,Chicken,Horse)
產(chǎn)品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 40kDa
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human KCNK9: 21-120/374 <Extracellular>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 KCNK9 or TASK-3 (TWIK-related Acid sensitive K+ channel) is a member of the potassium channel family of proteins that contain two-pore domain and four transmembrane domains. These channels are characterized as leak K+ channels that are sensitive to changes in the extracellular pH. The physiological functions of TASK channels are largely unknown; it has been proposed that they may be involved in the regulation of breathing, aldosterone secretion and anesthetic-mediated neuronal activity. They were found to act in neurons' membrane potential and in resting K+ currents.

Function:
pH-dependent, voltage-insensitive, background potassium channel protein.

Subcellular Location:
Membrane; Multi-pass membrane protein

Tissue Specificity:
Mainly found in the cerebellum. Also found in adrenal gland, kidney and lung.

DISEASE:
Defects in KCNK9 are the cause of Birk-Barel mental retardation dysmorphism syndrome (BIBAS) [MIM:612292]. A syndrome characterized by mental retardation, hypotonia, hyperactivity, and facial dysmorphism.

Similarity:
Belongs to the two pore domain potassium channel (TC 1.A.1.8)

SWISS:
Q9NPC2

Gene ID:
51305

Database links:

Entrez Gene: 428382 Chicken

Entrez Gene: 51305 Human

Omim: 605874 Human

SwissProt: Q9NPC2 Human

Unigene: 493037 Human



產(chǎn)品圖片
Sample: Cerebrum (Mouse) Lysate at 40 ug Cerebrum (Rat) Lysate at 40 ug Primary: Anti- KCNK9 (bs-5933R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 40 kD Observed band size: 48 kD
Sample: Adrenal gland (Mouse) Lysate at 40 ug Primary: Anti- KCNK9 (bs-5933R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 40 kD Observed band size: 48 kD
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