EZElisa™人极长链脂肪酸延长蛋白2（EZVL2）ELI
SA试剂盒-EZElisa™ Human Elongation of Very long Chain fatty Acids Protein 2 (ELOVL2) ELISA Kit- 询价
- Biogradetech
- 美国
- A-QEK04821-96wells
- 2025年09月29日
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- 文献和实验
- 技术资料
- 保存条件：
运输过程中保存：2-8℃
- 保质期：
1年
- 英文名：
EZElisa™ Human Elongation of Very long Chain fatty Acids Protein 2 (ELOVL2) ELISA Kit
- 库存：
100
- 供应商：
艾美捷科技
EZElisa™人极长链脂肪酸延长蛋白2（EZVL2）ELISA试剂盒，EZElisa™ Human Elongation of Very long Chain fatty Acids Protein 2 (ELOVL2) ELISA Kit，极长链脂肪酸延长蛋白2（EZVL2）ELISA试剂盒, Elongation of Very long Chain fatty Acids Protein 2 (ELOVL2) ELISA Kit
产品名称：EZElisa™ 人 Elongin A（EloA）ELISA试剂盒-EZElisa™ Human Elongation of Very long Chain fatty Acids Protein 2 (ELOVL2) ELISA Kit
产品货号：A-QEK04821-96wells
产品规格：96wells
Enzyme Immunoassay for the estimation of Elongation of Very long Chain fatty Acids Protein 2 (ELOVL2) in serum and plasma, tissue homogenates and other biological fluids.
种属：Human
检测方法：比色法
检测范围：
该EZElisa™人极长链脂肪酸延长蛋白2（EZVL2）ELISA试剂盒ELISA的特点包括：即用即用的操作步骤标准化和高重复性批次之间的一致性准确性和精确性经过七个点的验证，符合金环标准质量ELISA的要求，这是Biogradetech质量的基准标志。EZElisa™ ELISA试剂盒用于评估样品中的特定生物标志物，样品可以是血清
运输过程中保存：2-8℃
点击：EZElisa™ 人 Elongin A（EloA）ELISA试剂盒-EZElisa™ Human Elongation of Very long Chain fatty Acids Protein 2 (ELOVL2) ELISA Kit更多Biogradetech产品信息价格，货期，产品说明，百度搜“艾美捷科技”进入官网网站，查看具体产品且快速下单。
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文献和实验Mammalian Fatty Acid Elongases
Very long chain fatty acids confer functional diversity on cells by variations in their chain length and degree of unsaturation. Microsomal fatty acid elongation represents the major pathway for determining the chain length of saturated
Human Complement Components C4A and C4B Genetic Diversities: Complex Genotypes and Phenotypes
, C.Y. 2002b. Determining the one, two, three or four long and short loci of human complement C4 in a major histocompatibility complex haplotype encoding for C4A or C4B proteins. Am. J. Hum. Genet. 71:810‐822.
containing the human Lhcgr gene into a 170 kb BAC clone comprising the entire mouse orthologue. The methodology is based on the rationale to introduce a counter-selection cassette flanked by unique restriction sites and HAs for the insert, into the vector
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