推薦產品
生物源
rabbit
品質等級
共軛
unconjugated
抗體表格
affinity isolated antibody
抗體產品種類
primary antibodies
無性繁殖
polyclonal
形狀
buffered aqueous solution
分子量
63 kDa
物種活性
horse, rabbit, human
濃度
0.5 mg - 1 mg/mL
技術
western blot: suitable
NCBI登錄號
UniProt登錄號
運輸包裝
wet ice
儲存溫度
−20°C
目標翻譯後修改
unmodified
基因資訊
human ... ZFP91(80829)
免疫原
Synthetic peptide directed towards the N terminal region of human ZFP91
生化／生理作用
ZFP91 (ZNF757) is a member of zinc finger proteins that contain C2H2-type domains. It regulates the non-canonical NF-κB signaling induced by lymphotoxin-β receptor. An abundant expression of ZFP91 mRNA has been observed in prostate diseases including prostate cancer. ZFP91 may have a role in cell proliferation and survival and is a potential molecular marker for acute myelogenous leukemia.
序列
Synthetic peptide located within the following region: PQAAKSPSPVQGKKSPRLLCIEKVTTDKDPKEEKEEEDDSALPQEVSIAA
外觀
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
Lukasz Paschke et al.
Pathology oncology research : POR, 20(2), 453-459 (2013-11-26)
In search for novel molecular targets in benign prostate hyperplasia (BPH), a PCR Array based screening of 84 genes was performed. Of those, expression of ZFP91 (ZFP91 zinc finger protein) was notably upregulated. Limited data concerning the function of ZFP91
Motoko Unoki et al.
International journal of oncology, 22(6), 1217-1223 (2003-05-10)
To elucidate mechanisms leading to acute myelogenous leukemia (AML), to find sensitive markers and novel targets for drug therapy, and to allow choice of suitable chemotherapy for each affected individual, we previously compared expression of mRNA from mononuclear cells of
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