人TGM2 (Transglutaminase 2) knockout A549 cell裂解物
Human TGM2 (Transglutaminase 2) knockout A549 cell lysate
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TGM2 KO cell lysate available now. KO validated by Next Generation Sequencing, Western blot. Free of charge wild type control included. Knockout achieved by CRISPR/Cas9 X = 1 bp insertion 8 bp deletion Frameshift = 97%.
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ALPHA SUBUNIT, C polypeptide, EC 2.3.2.13, G alpha h, GNAH, GNAH G PROTEIN, G[a]h, Gh CLASS G ALPHA h, H POLYPEPTIDE, HEL-S-45, Protein-glutamine gamma-glutamyltransferase 2, TG 2, TG(C), TGC, TGC GUANINE NUCLEOTIDE BINDING PROTEIN, TGM2_HUMAN, TGase C, TGase H, TGase-2, TgaseII, Tissue transglutaminase, Transglutaminase 2 C polypeptide, Transglutaminase C, Transglutaminase H, Transglutaminase-2, epididymis secretory protein Li 45, tTG, tTGas
- WB
Lab
Western blot - Human TGM2 (Transglutaminase 2) knockout A549 cell lysate (AB261685)
Lane 1 : Wild-type A549 (Human lung carcinoma cell line) whole cell lysate 20 ug
Lane 2 : TGM2 knockout A549 (Human lung carcinoma cell line) whole cell lysate 20 ug
Lane 3 : HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate 20 ug
Lane 4 : HUVEC (Human umbilical vein endothelial cell line) whole cell lysate 20 ug
Lanes 1 - 4 : Merged signal (red and green). Green - ab2386 observed at 77 kDa. Red - loading control, ab181602, observed at 37 kDa.
ab2386 was shown to recognize in wild-type A549 cells as signal was lost at the expected MW in TGM2 knockout cell line ab261876 (knockout cell lysate ab261685). Additional cross-reactive bands were observed in the wild-type and knockout samples. Wild-type and TGM2 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% milk. ab2386 and ab181602 (Rabbit anti-GAPDH loading control) were incubated overnight at 4°C at 1 ug/ml and 1/20000 dilution respectively. Blots were developed with Goat anti-Mouse IgG H&L (IRDye® 800CW) preabsorbed ab216772 and Goat anti-Rabbit IgG H&L (IRDye® 680RD) preabsorbed ab216777 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Transglutaminase 2 antibody [CUB 7402] (<a href='/products/primary-antibodies/transglutaminase-2-antibody-cub-7402-ab2386'>ab2386</a>) at 1 µg/mL
Lane 1:
Wild-type A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2:
TGM2 knockout A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2:
Western blot - Human TGM2 (Transglutaminase 2) knockout A549 cell line (<a href='/products/cell-lines/human-tgm2-transglutaminase-2-knockout-a549-cell-line-ab261876'>ab261876</a>)
Lane 3:
HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 4:
HUVEC (Human umbilical vein endothelial cell line) whole cell lysate at 20 µg
Predicted band size: 77 kDa
Observed band size: 77 kDa
false
- WB
Lab
Western blot - Human TGM2 (Transglutaminase 2) knockout A549 cell lysate (AB261685)
Lane 1 : HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate 20 ug
Lane 2 : HUVEC (Human umbilical vein endothelial cell line) whole cell lysate 20 ug
Lane 3 : Wild-type A549 (Human lung carcinoma cell line) whole cell lysate 20 ug
Lane 4 : TGM2 knockout A549 (Human lung carcinoma cell line) whole cell lysate 20 ug
Lanes 1 - 4 : Merged signal (red and green). Green - ab64771 observed at 77 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab64771 was shown to specifically react with in wild-type A549 cells as signal was lost in TGM2 knockout cell line ab261876 (knockout cell lysate ab261685). Wild-type and TGM2 knockout samples were subjected to SDS-PAGE. ab64771 and ab8245 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1/5000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Anti-Transglutaminase 2 antibody (<a href='/products/unavailable/transglutaminase-2-antibody-ab64771'>ab64771</a>) at 1/5000 dilution
Lane 1:
HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 2:
HUVEC (Human umbilical vein endothelial cell line) whole cell lysate at 20 µg
Lane 3:
Wild-type A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 4:
TGM2 knockout A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 4:
Western blot - Human TGM2 (Transglutaminase 2) knockout A549 cell line (<a href='/products/cell-lines/human-tgm2-transglutaminase-2-knockout-a549-cell-line-ab261876'>ab261876</a>)
false
- NGS
Supplier Data
Next Generation Sequencing - Human TGM2 (Transglutaminase 2) knockout A549 cell lysate (AB261685)
Knockout achieved by CRISPR/Cas9; X = 1 bp insertion, 8 bp deletion; Frameshift = 97%
反应性数据
产品详情
Knockout cell lysate achieved by CRISPR/Cas9.
REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.
Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.
User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.
This product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.
规格
性能和储存信息
基因名称
基因编辑类型
基因编辑方法
敲除验证
运输条件
推荐的短期储存条件
推荐的长期储存条件
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Transglutaminase 2 plays roles in cell adhesion wound healing and the immune response. It mediates extracellular matrix stabilization through crosslinking structural proteins which is critical for tissue repair. The enzyme does not typically form a stable part of a large complex but interacts with fibronectin as a binding partner highlighting its role in cellular adhesion and migration. The enzymatic activity of transglutaminase 2 helps maintain tissue integrity by modifying extracellular and intracellular proteins.
Pathways
Transglutaminase 2 contributes significantly to the integrin-mediated signaling pathway and the apoptosis pathway. It assists in the modulation of cell-matrix interactions by crosslinking matrix proteins which is important for integrin signaling. During apoptosis transglutaminase 2 promotes cellular processes that lead to cell death via its involvement in nuclear condensation and DNA fragmentation. In these pathways proteins such as fibronectin and integrins interact with transglutaminase 2 facilitating its regulatory functions.
质量控制
STR 分析
CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
细胞培养
生物安全等级
EU: 1 US: 1
贴壁/悬浮
Adherent
性别
Male
Abcam Product Promise
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