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- 详细信息
- 文献和实验
- 技术资料
- 形态:
液态/粉状
- 保存条件:
-20℃保存
- 克隆性:
多克隆
- 标记物:
见说明书
- 适应物种:
人,大鼠,小鼠,兔
- 宿主:
Goat,Rabbit,Mouse
- 应用范围:
科研使用
- 浓度:
1mg/1ml
- 靶点:
来电咨询
1、制备抗原。
2、选择实验动物。
3、动物免疫。
4、试取血进行测试,看看是否成功免疫。
5、如果成功免疫,杀死实验动物,采集全部血清。
6、纯化出抗体。
7、鉴定抗体。包括纯度以及特异性。
ELISA夹心法测定中,HA与试剂抗体(捕获抗体和标记抗体)的结合,可通过Fc-Fc 和Fab-Fab两种结合方式干扰测定。正常情况下,在ELISA 夹心法中,待测抗原同时与捕获抗体和标记抗体结合,eIF3C Antibody形成了固相捕获抗体-待测抗原-标记抗体的复合物(如图1A所示)。在以Fc-Fc 的方式结合的机制中,HA的Fc 端结合到捕获抗体的Fc 段上,而HA的Fab 区域则结合到标记抗体的Fab 区域上,导致假阳性结果(如图1B所示)。在以Fab-Fab 结合方式的机制可引起假阳性或假阴性的结果,如HA的Fab区域通过分别结合捕获抗体的Fab区域和标记抗体的Fab 区域,eIF3C Antibody阻挡捕获抗体和标记抗体与待测抗原的结合,从而导致假阴性(如图1C所示);HA的F(ab’)2 通过同时结合捕获抗体的Fab区域和标记抗体的Fab区域,形成固相捕获抗体-HA-标记抗体复合物,如果标本中无待测抗原,HA就引起假阳性的结果。
eIF3C Antibody:xy-2112xy KT3 tagKT3 tag标签抗原
xy-2110xy VSV-G tag(vesicular stomatitis virus glycoprotein)VSV-G tag标签抗原
xy-1198xy HLA-DR(human leukoyte Antigen DR)HLA-DR抗原
xy-1279xy HLA-E人类白细胞抗原E
xy-1030xy Anti-HMGA1 (high mobility group AT-hook 1)高迁移率族蛋白A1抗原
xy-0556xy HMGA2 (high mobility group A2)高迁移率族蛋白A2抗原
xy-0827xy HO-1/HSP32 (Hemeo xygenase 1)血红素氧合酶-1/热休克蛋白-32抗原
xy-2075xy HO-1/HSP32(Hemeo xygenase 1)血红素氧合酶-1/热休克蛋白-32抗原
xy-1238xy HO-2(Heme oxygenase 2)血红素氧合酶-2抗原
xy-0928xy phospho-HP1/heterochromatin protein 1 (pTyr24)(fruit fly)异染色质蛋白1(磷酸化多肽)
xy-0930xy phospho-heterochromatin protein 1 (pTyr41)peptide异染色质蛋白1(磷酸化多肽)
xy-0991xy HPV18 E6人类乳头状瘤病毒18E6
xy-0992xy HPV16-E7/E7 protein(Human papillomavirus type 16)人类乳头状瘤病毒16抗原
xy-1808xy Hpt/HP(haptoglobin)结合珠蛋白/触珠蛋白抗原
xy-1071xy H-ras/Ras/Ras p21 peptide原癌基因H-ras抗原
xy-1409xy HSTF2/HSF2 peptide热休克转录因子2抗原
xy-2145xy Hrasls3/HREV107(HRAS like suppressor 3)HRAS样抑制因子3抗原
xy-1538xy HSP47(Heat shock protein-47)热休克蛋白-47抗原
xy-0889xy HSP-90 Alpha(Heat Shock Protein 90 Alpha )热休克蛋白90α抗体
xy-1387xy HSP-105 (heat sock protein-105)热休克蛋白HSP105抗原
xy-1271xy HtrA2/Omi peptide丝氨酸蛋白酶/线粒体丝氨酸蛋白酶多肽抗原
xy-1363xy Iba-1(Ionized calcium bindingadaptor molecule-1)离子钙接头蛋白抗原
xy-0898xy IFABP(Intestinal Fatty acid binding protein)小肠型脂肪酸结合蛋白抗原
xy-1031xy IFITM1 (interferon induced transmembrane protein 1)干扰素诱导跨膜蛋白1抗原
xy-1578xy human IFN- Alpha (Interferon Alpha )干扰素-α抗原(人)
xy-1463xy IFNGR1/CD119 peptide干扰素-gamma受体1抗原
xy-1108xy IGFBP-2 (Insulin-like Growth Factor Binding Protein 2)胰岛素样生长因子结合蛋白-2(多肽)
xy-1434xy IGFBP-3 (Insulin-like Growth Factor Binding Protein 3)C-term胰岛素样生长因子结合蛋白-3抗原
xy-1312xy IGF-IIBP3(Insulin like growth factor 2 mRNA binding protein 3)胰岛素样生长因子2 mRNA 结合蛋白3抗原
xy-1156xy IKB Beta (Inhibitor of KB)KB抑制蛋白β(多肽)
xy-1287xy IKB Alpha (Inhibitor of KB Alpha)KB抑制蛋白α抗原
xy-0767xy IL-12(Interleukin-12)白介素12抗原(白细胞介素-12)
xy-1789xy IL-12(Interleukin-12)human peptide白介素12抗原(人)
xy-2604xy IL-12R Beta2/IL12RB2 peptide白细胞介素-12受体β2抗原
xy-0560xy IL-13(Interleukin-13)白介素13抗原
xy-1771xy IL-14/Taxilin alpha白介素14抗原
xy-1829xy IL-15(Interleukin-15)白细胞介素-15抗原
xy-1830xy IL-16(Interleukin-16)白介素16抗原
xy-0768xy IL-16/LCF(interleukin-16)(Lymphocyte Chemotactic Factor)白细胞介素-16抗原
xy-0529xy IL-18/IGIF(Interleukin-18)白细胞介素-18/干扰素γ诱导因子
eIF3C Antibody单抗的最大优势是它的特异性、均一性、高效性和无限供应性。在免疫学、医学、生物学等领域的基础研究和临床医学上,包括对疾病(包括癌症)的诊断、预防和治疗等方面,均显示出巨大的生命力。
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文献和实验Generation of Antibody Molecules Through Antibody Engineering
been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional
The importance of antibody molecules was first recognized in the 1890s, when it was shown that immunity to tetanus and diphtheria was caused by antibodies against the bacterial exotoxins (1 ). Around the same time, it was shown that antisera
General comments: Antibodies, like most proteins, do not like to be freeze-thawed. Avoid repetitive freezing of your solution. The best way to store your antibody is to keep a high protein concentration (>1 mg/ml), add some protease
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