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11号染色体开放阅读框77抗体
AK18525
C11ORF77
Rabbit
Rat (predicted: Human,Mouse,Chicken,Dog,Pig,Cow,Horse,Rabbit,Sheep)
WB,IHC-P,IHC-F,IF,ELISA
多克隆
货号 纯度 规格 目录价 会员价 库存 数量 购买
AK18525-50ul 50ul 50ul ¥1380.00 登录查看
AK18525-100ul 100ul 100ul ¥2380.00 登录查看
AK18525-200ul 200ul 200ul ¥3480.00 登录查看
产品详情

公司产品仅供科研研究实验,不得用于临床!

商品详情:

英文名称:C11ORF77

中文名称:11号染色体开放阅读框77抗体

    名;Chromosome 11 open reading frame 77; FLJ32675; HARB1_HUMAN; HARBI1; Harbinger transposase derived 1; Harbinger transposase-derived nuclease; Putative nuclease HARBI1.

研究领域;肿瘤  细胞生物  免疫学  神经生物学  细胞周期蛋白

抗体来源;Rabbit

克隆类型;Polyclonal

交叉反应;Rat,  (predicted: Human, Mouse, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, )

产品应用;WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (石蜡切片需做抗原修复)

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

理论分子量;39kDa

细胞定位;细胞核 细胞浆

    状;Liquid

    度;1mg/ml

免 疫 原;KLH conjugated synthetic peptide derived from human C11ORF77/HARBI1: 11-100/349

    型;IgG

纯化方法;affinity purified by Protein A

缓 冲 液;0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

保存条件;Shipped at 4. Store at -20 °C 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.

产品介绍;HARBI1 is a 349 amino acid nuclear and cytoplasmic protein belonging to the HARBI1 family. Members of the HARBI1 family of proteins are highly conserved in humans to various bony fish. Considered a transposase-derived protein, HARBI1 may possess nuclease activity and is expressed in brain, eye, nerve tissue, kidney and lung. HARBI1 utilizes divalent metal cations as cofactors, interacts with NAIF1 and promotes translocation to the nucleus. HARBI1 is encoded by a gene located on human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

Function:

Transposase-derived protein that may have nuclease activity (Potential). Does not have transposase activity.

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