TGS1 Protein (AA 1-853) (Strep Tag)

Catalog No. ABIN3136894

This Recombinant TGS1 protein is expressed in Cell-free protein synthesis (CFPS).

Quick Overview for TGS1 Protein (AA 1-853) (Strep Tag) (ABIN3136894)

Target: TGS1 (Trimethylguanosine Synthase 1 (TGS1))

Protein Type: Recombinant

Origin: Mouse

Source: Cell-free protein synthesis (CFPS)

Application: ELISA, Western Blotting (WB), SDS-PAGE (SDS)

Purity: approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).

Grade: custom-made

Product Details

Protein Characteristics: AA 1-853

Purification tag / Conjugate: This TGS1 protein is labelled with Strep Tag.

Sequence: MCCEKWNHVA EMLLFIEDRE EEYKILCLCS RAFVEDRKLY NLGLKGYYVK SSGNNAGDQG TEEEEDGHSN GTAESHSPNE SDLDSEAKLM RSMGLPIQFG RMSSHENFEM SMNARNKAKV KQKRRKHQKR YLDEMVRESW RNDYEEDDLV VSDDPSSVEH CENNRTCEIQ SKAGSEVENL PVENTLAPKL EVPENWEKYW NEYGEGLLWQ SWQEKYPDQT LSSEPWNLPD TKEEWEQHYS QLYWYYLEQF QYWEAQGWTF TASQNCDKDV YTSHTEVDQN AESSLKADVM TFSSSPNIVE DEIPGSNDND HNEIITAINN ITVSAEKVEQ SQLDSSQHCD EPLSEITGKE CPASGGSDSC NGTPKENDIS ENRSSDQPAK ELQESSGTNK GKHRPHHNGA DGHESDDDPP EHKPSKVKRS HELDVDENPD SEVDDNGFLL GFKHGSGQKY GGIPNFSHRQ VRYLEKNVKY KSKYLDLRKQ MPVKSKHILF TEDSGKPFVV CKSKVRSKVE KFLKWVNERV DEETSQDSLS QNKMQDTCTS SDSEEQDMSL EKADNLMETR DPEPEKCQII SSATELEAEK SEVGSLVATV PENCSTEEIP NSPHAETEVE IKKKKKKNKN KKINDLPPEI ASVPELAKYW AQRYRLFSRF DDGIKLDKEG WFSVTPEKIA EHIAGRVSQA FRCDVVVDAF CGVGGNTIQF ALTGKRVIAI DIDPVKIDLA RNNAEVYGIA DKIEFICGDF LLLAPCLKAD VVFLSPPWGG PDYATAETFD IRTMMSPDGF EIFRLSQKIT NNIVYFLPRN ADIDQVASLA GLGGQVEIEQ NFLNNKLKTI TAYFGDLIRR PALLKTSTSE AEV
Sequence without tag. The proposed Strep-Tag is based on experience with the expression system. Our team may suggest an additional tag depending on the complexity of the protein. If you have a special request, please contact us..

Characteristics: Key Benefits:

• Made in Germany - from design to production - by highly experienced protein experts.
• Protein expressed with ALiCE® and purified in one-step affinity chromatography
• State-of-the-art algorithm used for plasmid design (Gene synthesis).

This protein is a predefined custom protein and will be made for the first time for your order. Our experts in the lab try to ensure that you receive soluble protein.

The big advantage of ordering our predefined custom proteins in comparison to ordering custom made proteins from other companies is that there is no financial obligation in case the protein cannot be expressed or purified.

Expression System:

• ALiCE®, our Almost Living Cell-Free Expression System is based on a lysate obtained from Nicotiana tabacum c.v.. This contains all the protein expression machinery needed to produce even the most difficult-to-express proteins, including those that require post-translational modifications.
• During lysate production, the cell wall and other cellular components that are not required for protein production are removed, leaving only the protein production machinery and the mitochondria to drive the reaction. During our lysate completion steps, the additional components needed for protein production (amino acids, cofactors, etc.) are added to produce something that functions like a cell, but without the constraints of a living system - all that's needed is the DNA that codes for the desired protein!

Concentration:

• The concentration of our recombinant proteins is measured using the absorbance at 280nm.
• The protein's absorbance will be measured against its specific reference buffer.
• We use the Expasy's ProtParam tool to determine the absorption coefficient of each protein.

Purification: One-step Strep-tag purification of proteins expressed in Almost Living Cell-Free Expression System (ALiCE®).

Application Details

Application Notes: In addition to the applications listed above we expect the protein to work for functional studies as well. As the protein has not been tested for functional studies yet we cannot offer a guarantee though.

Comment:

ALiCE®, our Almost Living Cell-Free Expression System is based on a lysate obtained from Nicotiana tabacum c.v.. This contains all the protein expression machinery needed to produce even the most difficult-to-express proteins, including those that require post-translational modifications.
During lysate production, the cell wall and other cellular components that are not required for protein production are removed, leaving only the protein production machinery and the mitochondria to drive the reaction. During our lysate completion steps, the additional components needed for protein production (amino acids, cofactors, etc.) are added to produce something that functions like a cell, but without the constraints of a living system - all that's needed is the DNA that codes for the desired protein!

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: The buffer composition is at the discretion of the manufacturer.
Standard Storage Buffer: PBS pH 7.4, 10 % Glycerol Might differ depending on protein.

Handling Advice: Avoid repeated freeze-thaw cycles.

Storage: -80 °C

Storage Comment: Store at -80°C.

Expiry Date: 12 months

Target Details

Target: TGS1 (Trimethylguanosine Synthase 1 (TGS1))

Alternative Name: Tgs1

Background: Trimethylguanosine synthase (EC 2.1.1.-) (Nuclear receptor coactivator 6-interacting protein) (PRIP-interacting protein with methyltransferase motif) (PIMT) (PIPMT),FUNCTION: Catalyzes the 2 serial methylation steps for the conversion of the 7-monomethylguanosine (m(7)G) caps of snRNAs and snoRNAs to a 2,2,7-trimethylguanosine (m(2,2,7)G) cap structure. The enzyme is specific for guanine, and N7 methylation must precede N2 methylation. Hypermethylation of the m7G cap of U snRNAs leads to their concentration in nuclear foci, their colocalization with coilin and the formation of canonical Cajal bodies (CBs). Plays a role in transcriptional regulation (By similarity). {ECO:0000250|UniProtKB:Q96RS0, ECO:0000269|PubMed:11517327}.

Molecular Weight: 96.8 kDa

UniProt: Q923W1

Pathways: Mitotic G1-G1/S Phases, Regulation of Lipid Metabolism by PPARalpha, Ribonucleoprotein Complex Subunit Organization