11号染色体开放阅读框74抗体

英文名称    C11orf74    

中文名称    11号染色体开放阅读框74抗体    

别    名    Chromosome 11 open reading frame 74; FLJ38678; HEPIS; Hypothetical protein LOC119710; Protein HEPIS; CK074_HUMAN.    

说 明 书    0.2ml      

研究领域    心血管  细胞生物  免疫学  神经生物学      

抗体来源    Rabbit    

克隆类型    Polyclonal    

交叉反应    Human, Mouse, Rat,     

产品应用    WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 （石蜡切片需做抗原修复）11号染色体开放阅读框74抗体 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.    

分 子 量    25kDa    

性    状    Lyophilized or Liquid    

浓    度    1mg/1ml    

免 疫 原    KLH conjugated synthetic peptide derived from human C11orf74    

亚    型    IgG    

纯化方法    affinity purified by Protein A    

储 存 液    Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4    

保存条件    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.    

11号染色体开放阅读框74抗体产品介绍    background:

C11orf74, also known as FLJ38678, is a 123 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and β thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.    

11号染色体开放阅读框74抗体

hz-6709R CaIPLA2/PLA2G6  胞浆钙独立磷脂酶A2抗体

hz-6710R Netrin G1 ligand  轴突生长诱向因子G1配体抗体

hz-6711R Netrin 4  轴突生长诱向因子4抗体

hz-6712R PAX4  配对盒同源基因4抗体

hz-6713R Laminin 5  层粘连蛋白5(laminin γ2)抗体

hz-6714R UGCGL2  二磷酸葡萄糖神经酰胺葡萄糖基转移酶2抗体

hz-6715R UGDH/UDPGDH  尿苷二磷酸葡萄糖脱氢酶抗体

hz-6716R Uricase  尿酸酶

hz-6717R NALP2/PAN1/PYPAF2  富含亮氨酸重复结构域蛋白2抗体

hz-6718R Dystrophin/DMD  肌营养不良蛋白

hz-6719R LGI1/ETL1  富含亮氨酸胶质瘤失活蛋白1抗体

hz-6720R GANAB/alpha Glucosidase II  α葡萄糖苷酶2抗体

hz-6721R NLG1/KIRREL2  肾病样蛋白1抗体

hz-6722R MAPK organizer 1/Morg1  丝裂原活化蛋白激酶组织蛋白1抗体

hz-6723R PNPLA6/NTE  含patatin样磷脂酶6抗体

hz-6724R OTC  鸟氨酸氨基甲酰转移酶抗体

hz-6725R Desmoglein 1/DSG1  桥粒芯糖蛋白1

hz-6727R CAMKIV/CAMK4  钙/钙调蛋白依赖性蛋白激酶4抗体

hz-6728R phospho-CAMK4(Thr196 + Thr200)  磷酸化钙/钙调蛋白依赖性蛋白激酶4抗体

hz-6730R LBP1/Upstream Binding Protein 1  上游结合蛋白1抗体

hz-6732R SDF4  基质细胞衍生因子4抗体（钙结合蛋白）

hz-6733R SECTM1  分泌和跨膜蛋白1抗体

hz-6734R SERBP1  纤溶酶原激活物抑制剂1 RNA结合蛋白抗体

hz-6735R SFR19  剪接因子，精氨酸/丝氨酸丰富19

hz-6736R SOX11  转录因子SOX-11蛋白抗体

hz-6737R SVH/ARMC10  肝癌蛋白剪接变异体蛋白抗体

hz-6738R THRSP  甲状腺激素反应蛋白抗体

hz-6739R TIMM17A  线粒体内膜转位酶抗体

hz-6740R TMhz49  跨膜蛋白49抗体

hz-6741R TMS1/ASC  凋亡相关斑点样蛋白ASC抗体

hz-6742R TPD52/Prostate and colon associated protein  前列腺癌和结肠癌相关蛋白

hz-6743R TPD54/TPD52L2  肿瘤蛋白D54蛋白抗体

hz-6744R TRIM47  星形细胞瘤高表达蛋白抗体（环指蛋白100）

hz-6745R TSP50  肿瘤/睾丸抗原20抗体

hz-6746R TULP2/CT65/Cancer testis antigen 65  肿瘤/睾丸抗原65