产品中心 / 产品类型 / 细胞系&裂解液 / KO细胞系

MGAT1 with GNT1 Knockout 293F Cell Line, Homozygous (RM50162)

Genome sequence analysis of PCR products from parental (WT) and MGAT1 with GNT1 knockout (KO) 293F cells, using sanger sequencing.

All(1)|
货号: RM50162
促销价:   ¥10000
货    期:现货产品
抗体定制服务咨询

文献引用 (0)

详细信息

靶点
MGAT1,GNT1
细胞系
293F
突变描述
MGAT1,GNT1 Knockout cell line is engineered from 293F cell line with Gene-Editing Technology.
Allele-1:exon3 was deleted,Allele-2:85bp deletion in exon3(GNT1)
Allele-1:53bp deletion in exon1;Allele-2:52bp deletion in exon1(MGAT1)

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 line and 1 vial knockout cell line
细胞数目
1~5x106 cells/vial.
使用方法
Upon arrival, it should be maintained in DMEM medium with 10%(v/v) fetal bovine serum and 100U penicillin-streptomycin, at 37℃ with 5% CO2 condition.
1. Thaw the vial in 37℃ water bath ,and shake it to melt as soon as possible.
2. Transfer the cell suspension to a 15mL conical tube with pre-warmed 5mL complete me-
    dium and centrifuge 1000rpm for approximately 5 minutes at room temperature.
3. Remove and discard the supernatant.
4. Resuspend the cell pellet with 1mL pre-warmed complete medium and seed in 10cm dish.
5. Add 8-10mL of complete medium.
6. Incubate the culture at 37℃ incubator with 5% CO2.
7. A subcultivation ratio of 1:2-1:4 is recommended.
物种
Human
保存条件
Stored in liquid nitrogen for a long time less than -130℃. Minimizing freeze-thaw cycles.
运输条件
Dry ice

背景信息

There are believed to be over 100 different glycosyltransferases involved in the synthesis of protein-bound and lipid-bound oligosaccharides. UDP-N-acetylglucosamine:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I is a medial-Golgi enzyme essential for the synthesis of hybrid and complex N-glycans. The protein, encoded by a single exon, shows typical features of a type II transmembrane protein. The protein is believed to be essential for normal embryogenesis. Several variants encoding the same protein have been found for this gene.

基因ID
Swiss Prot
别名
GnTI; MGAT; GLCT1; GLYT1; GNT-1; GNT-I; GLCNAC-TI; MGAT1
>