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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。
商品属性：
产品名称 1号染色体开放阅读框63抗体 货号 BJ011569 英文名称 NPD014 浓 度 1mg/ml 研究领域 细胞生物 神经生物学 ���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 34kDa 用途 仅供科研研究实验
产品名称
1号染色体开放阅读框63抗体
货号
BJ011569
英文名称
NPD014
浓 度
1mg/ml
研究领域
细胞生物 神经生物学
���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
34kDa
用途
仅供科研研究实验
商品介绍：
别 名 C1orf63; Chromosome 1 open reading frame 63; DJ465N24.2.1; Hypothetical protein LOC57035; RP3 465N24.4; UPF0471 protein C1orf63; CA063_HUMAN. 交叉反应；Human, Mouse, Rat, 产品应用；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. 免 疫 原；KLH conjugated synthetic peptide derived from human NPD014: 4-100/290 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 C1orf63 gene product has been provisionally designated C1orf63 pending further characterization.
别 名 C1orf63; Chromosome 1 open reading frame 63; DJ465N24.2.1; Hypothetical protein LOC57035; RP3 465N24.4; UPF0471 protein C1orf63; CA063_HUMAN.
交叉反应；Human, Mouse, Rat,
产品应用；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.
免 疫 原；KLH conjugated synthetic peptide derived from human NPD014: 4-100/290
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 C1orf63 gene product has been provisionally designated C1orf63 pending further characterization.
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磷脂酰丝氨酸脱羧酶PISD抗体 PISD 植物蔗糖磷酸合成酶（sucrose phosphate synthase）活性 锚蛋白重复结构域蛋白37抗体 ANKRD37 甲基柠檬酸合酶(MCS）测试盒 FAM150A蛋白抗体 FAM150A 细胞甘肽合成酶活性比色法定量检测试剂盒 FBXL22蛋白抗体 FBXL22 小鼠降钙素(CT)elisa检测试剂盒 丝裂原活化蛋白激酶2重组兔单克隆抗体 ERK2 内切-β-1，4-葡聚糖酶（Cx）测试盒 信号转导和转录激活因子5抗体 STAT5 大鼠促甲状腺素释放(TRH)elisa检测试剂盒 蛋白磷酸酶3调节亚基C抗体 PPP3CC 台桌清洁剂（饭桌、工作台、学生课桌椅等）a 胆固醇调节元件结合蛋白1抗体 SREBP1 鹅降钙素(CT)elisa分析检测试剂盒 血管非炎症分子1抗体 VNN1 非位素AP化学发光法DNA斑点杂交试剂盒 胎球蛋白A Fetuin A/AHSG 小鼠半乳糖凝集素7(GAL7)elisa检测试剂盒 PE标记小鼠CD22单克隆抗体 mouse CD22/PE 小鼠糖原合酶激酶3α(GSK3α)elisa检测试剂盒 Rabbit Anti-Acetyl-Histone H3 (Lys14) antibody 大鼠窖蛋白Caveolin1(Cav-1)elisa检测试剂盒 1号染色体开放阅读框167抗体 C1orf167 组织磷酸二酯酶2（PDE2）活性荧光定量检测试剂盒 26S蛋白酶调节亚型7抗体 GTPBP3 人妊娠相关蛋白A（PAPP-A）elisa检测试剂盒 1号染色体开放阅读框63抗体TMEFF1蛋白抗体 TMEFF1 研究领域； 细胞生物 表观遗传学 硒蛋白SECIS结合蛋白2抗体 SECISBP2 研究领域；细胞生物 发育生物学 信号转导 干细胞 表观遗传学 快速周期调节蛋白E5抗体 SPDYE5 研究领域；细胞生物 细胞周期蛋白 ASCL2蛋白抗体 ASCL2 研究领域；细胞生物 发育生物学 信号转导 干细胞 表观遗传学
磷脂酰丝氨酸脱羧酶PISD抗体 PISD
植物蔗糖磷酸合成酶（sucrose phosphate synthase）活性
锚蛋白重复结构域蛋白37抗体 ANKRD37
甲基柠檬酸合酶(MCS）测试盒
FAM150A蛋白抗体 FAM150A
细胞甘肽合成酶活性比色法定量检测试剂盒
FBXL22蛋白抗体 FBXL22
小鼠降钙素(CT)elisa检测试剂盒
丝裂原活化蛋白激酶2重组兔单克隆抗体 ERK2
内切-β-1，4-葡聚糖酶（Cx）测试盒
信号转导和转录激活因子5抗体 STAT5
大鼠促甲状腺素释放(TRH)elisa检测试剂盒
蛋白磷酸酶3调节亚基C抗体 PPP3CC
台桌清洁剂（饭桌、工作台、学生课桌椅等）a
胆固醇调节元件结合蛋白1抗体 SREBP1
鹅降钙素(CT)elisa分析检测试剂盒
血管非炎症分子1抗体 VNN1
非位素AP化学发光法DNA斑点杂交试剂盒
胎球蛋白A Fetuin A/AHSG
小鼠半乳糖凝集素7(GAL7)elisa检测试剂盒
PE标记小鼠CD22单克隆抗体 mouse CD22/PE
小鼠糖原合酶激酶3α(GSK3α)elisa检测试剂盒
Rabbit Anti-Acetyl-Histone H3 (Lys14) antibody
大鼠窖蛋白Caveolin1(Cav-1)elisa检测试剂盒
1号染色体开放阅读框167抗体 C1orf167
组织磷酸二酯酶2（PDE2）活性荧光定量检测试剂盒
26S蛋白酶调节亚型7抗体 GTPBP3
人妊娠相关蛋白A（PAPP-A）elisa检测试剂盒
1号染色体开放阅读框63抗体TMEFF1蛋白抗体 TMEFF1 研究领域； 细胞生物 表观遗传学 硒蛋白SECIS结合蛋白2抗体 SECISBP2 研究领域；细胞生物 发育生物学 信号转导 干细胞 表观遗传学 快速周期调节蛋白E5抗体 SPDYE5 研究领域；细胞生物 细胞周期蛋白 ASCL2蛋白抗体 ASCL2 研究领域；细胞生物 发育生物学 信号转导 干细胞 表观遗传学