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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Recombinant Human Fatty acid desaturase 1 protein (1-121AA)
- 亚型:
IgG
- 形态:
Liquid
- 保存条件:
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性:
Polyclonal
- 标记物:
Biotin
- 适应物种:
Human
- 保质期:
6个月
- 抗原来源:
Homo sapiens (Human)
- 目录编号:
O60427
- 级别:
优
- 库存:
200
- 供应商:
武汉华美生物工程有限公司
- 宿主:
Rabbit
- 应用范围:
ELISA
- 浓度:
>95%,Protein G purified
- 靶点:
FADS1
- 抗体英文名:
FADS1 Antibody, Biotin conjugated
- 抗体名:
FADS1;FADSD5;Acyl-CoA;8-3-desaturase;Delta(5 fatty acid desaturase;D5D;Delta(5 desaturase;Delta-5 desaturase;Fatty acid desaturase 1
- 规格:
100μg/50μg
| 规格: | 100μg | 产品价格: | ¥1320.0 |
|---|---|---|---|
| 规格: | 50μg | 产品价格: | ¥880.0 |
保存缓冲液
Preservative: 0.03% Proclin 300Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
功能
Isoform 2 does not exhibit any catalytic activity toward 20:3n-6, but it may enhance FADS2 activity (By similarity). Isoform 1 is a component of a lipid metabolic pathway that catalyzes biosynthesis of highly unsaturated fatty acids (HUFA) from precursor essential polyunsaturated fatty acids (PUFA) linoleic acid (LA) (18:2n-6) and alpha-linolenic acid (ALA) (18:3n-3). Catalyzes the desaturation of dihomo-gamma-linoleic acid (DHGLA) (20:3n-6) and eicosatetraenoic acid (20:4n-3) to generate arachidonic acid (AA) (20:4n-6) and eicosapentaenoic acid (EPA)(20:5n-3), respectively.风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验特异性的选择主要需要考虑四个方面:蛋白特异性、种属特异性、实验方法特异性、标记物的特异性。 (1)蛋白特异性 针对需要检测的蛋白查找抗体,几个细节要区分,重组表达的蛋白和内源性蛋白的检测,对抗体的要求是不一样的,注意查看抗体说明书的检测说明。如果重组蛋白不是全长表达,则需要注意抗体的免疫原区域是否在重组蛋白区域内。内源性蛋白最好能清楚其剪切与修饰的方式,特殊表型的蛋白需要进行序列比对,并结合抗体免疫原序列,查看交叉反应的情况。磷酸化蛋白检测需要确定具体位点,不同位点的磷酸化意味
Preparation of nucleic acid probes
Digoxigenin is a plant steroid (obtained from Dig i- talis plants) to which a specific antibody has been raised. The digoxigenin-specific antibody permits detection of nucleic acid molecules which have incorporated nucleotides containing the digoxigenin
of fluorochrome- or enzyme-conjugated avidin or antibody molecules (4 ,5 ,9 ,10 ), followed by fluorescence microscopy or brightfeld visualization of enzyme reaction products. Particularly, rapidity, simplicity, and cost-effectiveness have made the PRINS
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