商品属性：
产品名称 1号染色体开放阅读框189抗体 货号 BJ005133 英文名称 C1orf189 浓 度 1mg/ml 研究领域 细胞生物 神经生物学 细胞定位 细胞核 细胞浆 抗体来源 Rabbit 性 状 Liquid 克隆类型 Polyclonal 亚 型 IgG 理论分子量 12kDa 用途 仅供科研研究实验
产品名称
1号染色体开放阅读框189抗体
货号
BJ005133
英文名称
C1orf189
浓 度
1mg/ml
研究领域
细胞生物 神经生物学
细胞定位
细胞核 细胞浆
抗体来源
Rabbit
性 状
Liquid
克隆类型
Polyclonal
亚 型
IgG
理论分子量
12kDa
用途
仅供科研研究实验
商品介绍：
别 名 Chromosome 1 open reading frame 189; Uncharacterized protein C1orf189; CA189_HUMAN. 交叉反应；(predicted: Human, Mouse, ) 产品应用；WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （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. 免 疫 原；KLH conjugated synthetic peptide derived from human C1orf189 : 11-80/101 亚 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： Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf189 gene product has been provisionally designated C1orf189 pending further characterization.
别 名 Chromosome 1 open reading frame 189; Uncharacterized protein C1orf189; CA189_HUMAN.
交叉反应；(predicted: Human, Mouse, )
产品应用；WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （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.
免 疫 原；KLH conjugated synthetic peptide derived from human C1orf189 : 11-80/101
亚 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：
Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf189 gene product has been provisionally designated C1orf189 pending further characterization.
什么是一抗：
单克隆抗体和多克隆抗体都是我们实验中常用的抗体产品。他们在识别的抗原表位、生产和应用等方面有一些区别。 ✓多克隆抗体（polyclonal antibody, pAb）：用一种包含多种抗原决定簇的抗原动物，可刺激机体多个 B 细胞克隆产生针对多种抗原表位的抗体。 ✓单克隆抗体（monoclonal antibodies, mAb）：由单一 B 细胞克隆产生的识别一种抗原表位的抗体。 双特异性抗体实验流程 ：
公司正在出售的产品：
碱性成纤维细胞生长因子/FGF2抗体 FGF2 组蛋白H2A-K9乙酰化检测试剂盒 紧密连接蛋白17抗体 Claudin 17 人B细胞生长因子(BCGF)elisa检测试剂盒 5-羟色胺受体1F抗体 5HT1F Receptor 细胞培养抗支原体污染试剂盒 9号染色体开放阅读框169抗体 C9orf169 沙丁胺醇ELISA检测试剂盒 脑转录因子4蛋白抗体 BRN4 大鼠抗精子抗体(AsAb)elisa分析检测试剂盒 铁氧化还原蛋白还原酶抗体 Ferredoxin Reductase 细胞总氨基酸含量比色法定量检测试剂盒 S100B蛋白抗体 S100B 组织甘油-3-磷酸脱氢酶-1（Glycerol-3-Phosphate Dehydrogenase-1）活性光谱法定量检测试剂盒 RBNS5蛋白抗体 Rabenosyn 5 大鼠低密度脂蛋白受体(LDLR)elisa检测试剂盒 突触融合蛋白3抗体 STX3 小鼠坏死因子相关凋亡诱导配体受体3(TRAIL-R3)elisa检测试剂盒 凝集素样蛋白AGRNL抗体 FLJ39155 人雌三醇(E3)elisa分析检测试剂盒 FOXD4L1蛋白抗体 FOXD4L1 小鼠Ⅳ型胶原(COL4)elisa检测试剂盒 GTP结合蛋白4抗体（慢性肾功能衰竭蛋白） GTPBP4 聚糖二氨基亚甲基二氧基苯（DMB）荧光标记试剂盒 胰肠源结构域转录因子抗体 ISX/Intestine specific homeobox 载玻片细胞CDK6蛋白表达NBT显色光学显微镜检测试剂盒 乙酰化组蛋白H2B K15抗体 Histone H2B (acetyl K15) 几丁质酶测试盒 1号染色体开放阅读框189抗体复合素3抗体 CPLX3 研究领域；细胞生物 神经生物学 信号转导 原钙粘蛋白γA2抗体 PCDHGA2 研究领域；信号转导 细胞粘附分子 细胞骨架 细胞膜蛋白 去整合素样金属蛋白酶28抗体 ADAM28 研究领域； 细胞生物 信号转导 Kelch样蛋白21抗体 KLHL21 研究领域； 细胞生物 信号转导 表观遗传学
碱性成纤维细胞生长因子/FGF2抗体 FGF2
组蛋白H2A-K9乙酰化检测试剂盒
紧密连接蛋白17抗体 Claudin 17
人B细胞生长因子(BCGF)elisa检测试剂盒
5-羟色胺受体1F抗体 5HT1F Receptor
细胞培养抗支原体污染试剂盒
9号染色体开放阅读框169抗体 C9orf169
沙丁胺醇ELISA检测试剂盒
脑转录因子4蛋白抗体 BRN4
大鼠抗精子抗体(AsAb)elisa分析检测试剂盒
铁氧化还原蛋白还原酶抗体 Ferredoxin Reductase
细胞总氨基酸含量比色法定量检测试剂盒
S100B蛋白抗体 S100B
组织甘油-3-磷酸脱氢酶-1（Glycerol-3-Phosphate Dehydrogenase-1）活性光谱法定量检测试剂盒
RBNS5蛋白抗体 Rabenosyn 5
大鼠低密度脂蛋白受体(LDLR)elisa检测试剂盒
突触融合蛋白3抗体 STX3
小鼠坏死因子相关凋亡诱导配体受体3(TRAIL-R3)elisa检测试剂盒
凝集素样蛋白AGRNL抗体 FLJ39155
人雌三醇(E3)elisa分析检测试剂盒
FOXD4L1蛋白抗体 FOXD4L1
小鼠Ⅳ型胶原(COL4)elisa检测试剂盒
GTP结合蛋白4抗体（慢性肾功能衰竭蛋白） GTPBP4
聚糖二氨基亚甲基二氧基苯（DMB）荧光标记试剂盒
胰肠源结构域转录因子抗体 ISX/Intestine specific homeobox
载玻片细胞CDK6蛋白表达NBT显色光学显微镜检测试剂盒
乙酰化组蛋白H2B K15抗体 Histone H2B (acetyl K15)
几丁质酶测试盒
1号染色体开放阅读框189抗体复合素3抗体 CPLX3 研究领域；细胞生物 神经生物学 信号转导 原钙粘蛋白γA2抗体 PCDHGA2 研究领域；信号转导 细胞粘附分子 细胞骨架 细胞膜蛋白 去整合素样金属蛋白酶28抗体 ADAM28 研究领域； 细胞生物 信号转导 Kelch样蛋白21抗体 KLHL21 研究领域； 细胞生物 信号转导 表观遗传学