产品和服务 / 产品类型 / 细胞系&裂解液 / KO细胞裂解液

SLC38A8 Knockout 293T Cell Lysate, Homozygous (RM50104)

Genome sequence analysis of PCR products from parental (WT) and SLC38A8 knockout (KO) 293T cells, using sanger sequencing.

All(1)|
货号: RM50104
促销价:   ¥4700
货    期:现货产品
抗体定制
服务咨询
|
扫码下单
享受积分

详细信息

靶点
SLC38A8
细胞系
293T
突变描述
SLC38A8 Knockout cell line is engineered from 293T cell line with Gene-Editing Technology.
Allele-1:158bp deletion in exon1
Allele-2:158bp 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

This gene encodes a putative sodium-dependent amino-acid/proton antiporter. The protein has eleven transmembrane domains, an extracellular N-terminus and an intracellular C-terminal tail. The protein is a member of the SLC38 sodium-coupled neutral amino acid transporter family of proteins. Mutations in this gene result in foveal hypoplasia with or without optic nerve misrouting and/or anterior segment dysgenesis.