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Rabbit Anti-SLC22A18AS/AP Conjugated antibody (bs-21210R-AP)
訂購熱線:400-901-9800
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訂購QQ:  400-901-9800
技術(shù)支持:techsupport@m.p2b3.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-21210R-AP
英文名稱1 Rabbit Anti-SLC22A18AS/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)標(biāo)記的溶質(zhì)載體家族22成員18樣蛋白抗體
別    名 Beckwith-Wiedemann region 1B; Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein; Beckwith-Wiedemann syndrome chromosome region 1, candidate b; BWR1B; BWR1B_HUMAN; BWSCR1B; ORCTL2S; Organic cation transporter like 2 antisense; Organic cation transporter-like protein 2 antisense protein; OTTHUMP00000229183; p27-Beckwith-Wiedemann region 1 B; p27-BWR1B; SLC22A18AS; SLC22A1LS; Solute carrier family 22 (organic cation transporter), member 1 like antisense; Solute carrier family 22 (organic cation transporter), member 18 antisense; Solute carrier family 22 member 1-like antisense protein; Solute carrier family 22 member 18 antisense protein.  
規(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 細(xì)胞生物  免疫學(xué)  轉(zhuǎn)運(yùn)蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, )
產(chǎn)品應(yīng)用 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 27kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SLC22A18AS
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 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:
SLC22A18AS (Solute Carrier Family 22 Member 18 Antisense) is a Protein Coding gene. Diseases associated with SLC22A18AS include Beckwith-Wiedemann Syndrome.

Tissue Specificity:
Most abundantly expressed in gastrointestinal tissues. Expressed at lower levels in kidney and placenta. Expressed in fetal brain, liver, placenta, kidney and lung.

Database links:

Entrez Gene: 5003 Human

Omim: 603240 Human

SwissProt: Q8N1D0 Human

Unigene: 300076 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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