产品和服务 / 产品类型 / 细胞系&裂解液 / KO细胞裂解液

NDUFB11 Knockout HeLa Cell Lysate, Homozygous (RM50005)

Genome sequence analysis of PCR products from parental (WT) and NDUFB11 knockout (KO) HeLa cells, using sanger sequencing.

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货号: RM50005
促销价:   ¥4700
货    期:现货产品
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详细信息

靶点
NDUFB11
细胞系
HeLa
突变描述
NDUFB11 Knockout cell line is engineered from HeLa cell line with Gene-Editing Technology.
Allele-1:86bp deletion in exon1
Allele-2:85bp deletion in exon1

Mammalian cells such as human, rat and mouse cells are normally diploid with two alleles.
Homozygote: both alleles were knocked out, mRNA has no signal, no expression of proteins.
Heterozygote: only one allele was knocked out, the mRNA transcript levels was decreased compared to wild type, and the protein expression levels was also lower than that of the wild type.
敲除验证
Sanger Sequencing
产品组成
1 vial parental cell Lysate and 1 vial knockout cell Lysate
裂解液量
50μL, 2μg/μL.
使用方法
To be used as WB control. Lysate is supplied in 1× SDS sample buffer (2% SDS, 60 mM
Tris-HCl pH 6.8, 10% Glycerol, 0.02% Bromophenol blue, 60 mM beta-mercaptoethanol).
Lysate should be boiled for 3 - 5 minutes before loading onto gel.
物种
Human
保存条件
Lysate is stable for 12 months when stored at -20℃. Minimizing freeze-thaw cycles.
运输条件
4℃

背景信息

The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is located at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to ubiquinone. Mutations in the human gene are associated with linear skin defects with multiple congenital anomalies 3 and mitochondrial complex I deficiency.

基因ID
Swiss Prot
别名
ESSS; Np15; P17.3; NP17.3; CI-ESSS; MC1DN30; NDUFB11