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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10133 |
3'-Azido-3'-deoxy-5-methylcytidine
|
Antiviral; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
3'-Azido-3'-deoxy-5-methylcytidine 抑制 HIV-1 逆转录酶 (EC50 = 0.06 μM),是异嗜性鼠白血病相关逆转录病毒 (XMRV, CC50 = 43.5 μM) 的有效抑制剂。 | |||
T17515 |
Azido-PEG5-azide
叠氮-五聚乙二醇-叠氮 |
Others; PROTAC Linker | Others; PROTAC |
Azido-PEG5-azide 是一种属于 PEG 类的 PROTAC linker,可用于 PROTAC 分子的合成。 | |||
T38751 |
Azido-PEG5-S-methyl ethanethioate
Azido-PEG5-S-methyl ethanethioate |
Others | Others |
Azido-PEG5-S-methyl ethanethioate is a polyethylene glycol (PEG)-based linker utilized for the synthesis of proteolysis targeting chimeras (PROTACs). | |||
T19133 |
3'-Azido-3'-deoxy-5-fluorocytidine
|
Others | Others |
3'-Azido-3'-deoxy-5-fluorocytidine is a cytidine derivative. | |||
T32816 |
L-Lysine, 5'-ester with 3'-azido-3'-deoxythymidine
|
Others | Others |
L-Lysine, 5'-ester with 3'-azido-3'-deoxythymidine is a bioactive chemical. | |||
T14454 |
Azido-PEG5-acid
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Azido-PEG5-acid is a non-cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs), such as the conjugate CPT-APO (CPT: Camptothecin. | |||
T14456 |
Azido-PEG5-alcohol
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Azido-PEG5-alcohol, a non-cleavable 5 unit polyethylene glycol (PEG) ADC linker, finds application in the synthesis of antibody-drug conjugates (ADCs)[1]. Additionally, it serves as a PEG-based PROTAC linker for the synthesis of PROTACs[2]. | |||
T17516 |
Azido-PEG5-maleimide
|
Others | Others |
Azido-PEG5-maleimide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T14461 |
Azido-PEG5-CH2CO2H
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Azido-PEG5-CH2CO2H is a cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T14458 |
Azido-PEG5-Boc
|
Others | Others |
Azido-PEG5-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
TNU1255 |
5’-Azido-5’-deoxyadenosine
|
Others | Others |
5'-Azido-5'-deoxyadenosine is a Nucleoside Derivative - 5'-Modified nucleoside; Azido-nucleoside. | |||
TNU1149 |
5’-Azido-5’-deoxythymidine
|
Others | Others |
Nucleoside Derivatives - 5’-Modified nucleosides, Azido-nucleosides; Drugs and Inhibitors; Inhibitor of mycobacterium tuberculosis monophosphate kinase (TMPKmt) | |||
TNU1166 |
5’-Azido-5’-deoxyuridine
|
Others | Others |
Nucleoside Derivatives - Azido nucleosides; 5’-Modified nucleosides | |||
TNU1256 |
5’-Azido-2’,5’-dideoxyadenosine
|
Others | Others |
5'-Azido-2',5'-dideoxyadenosine is a Nucleoside Derivative - 5'-Modified nucleoside; Azido-nucleoside. | |||
T14459 |
Azido-PEG5-CH2CO2-NHS
|
Others | Others |
Azido-PEG5-CH2CO2-NHS is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T14460 |
Azido-PEG5-CH2CO2-PFP
|
Others | Others |
Azido-PEG5-CH2CO2-PFP is a polyethylene glycol (PEG) and Alkyl/ether-based linker compound. It serves as a key component in the synthesis of proteolysis-targeting chimeras (PROTACs), a class of molecules used for targeted protein degradation[1]. | |||
T14457 |
Azido-PEG5-amine
|
Others | Others |
Azido-PEG5-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17517 |
Azido-PEG5-triethoxysilane
|
Others | Others |
Azido-PEG5-triethoxysilane serves as a PEG-based PROTAC linker for the synthesis of PROTACs[1]. | |||
T14462 |
Azido-PEG5-NHS ester
|
Others | Others |
Azido-PEG5-NHS ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
TNU1152 |
5’-Azido-2’,5’-dideoxyuridine
|
Others | Others |
5'-Azido-2',5'-dideoxyuridine is a Nucleoside Derivative - 5'-Modified nucleoside, Azido-nucleoside. | |||
T14464 |
Azido-PEG5-succinimidyl carbonate
|
Others | Others |
Azido-PEG5-succinimidyl carbonate is a polyethylene glycol (PEG) derivative with a linked succinimidyl carbonate and azido group. It serves as a PEG-based PROTAC linker for the synthesis of PROTACs[1]. | |||
TNU1146 |
5’-Azido-5’-deoxy-5-methyluridine
|
Others | Others |
5'-Azido-5'-deoxy-5-methyluridine is a Nucleoside Derivative - 5'-Modified nucleoside, Azido-nucleoside. | |||
T14463 |
Azido-PEG5-PFP ester
|
Others | Others |
Azido-PEG5-PFP ester is a Polyethylene Glycol (PEG) and Alkyl/ether-based Proteolysis Targeting Chimera (PROTAC) linker, commonly employed for PROTAC synthesis [1]. | |||
T40616 |
8-Azido-ATP
8-Azidoadenosine 5'-triphosphate,8-N3-ATP,8-Azido-ATP |
Others | Others |
8-Azido-ATP is a nucleotide analog that demonstrates photo-reactivity properties. It offers utility in the precise labeling and identification of proteins, particularly those involved in DNA-dependent RNA polymerase activity. | |||
TNU1129 |
5’-Azido-2’,5’-dideoxy-2’-fluorouridine
|
Others | Others |
Nucleoside Derivatives - Azido-nucleosides, 5’-Modified nucleosides, 2’-Modified nucleosides, Fluoro-modified nucleosides | |||
T14455 |
Azido-PEG5-Ala-Ala-Asn-PAB
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Azido-PEG5-Ala-Ala-Asn-PAB is a cleavable 5-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
TNU1132 |
5’-Azido-5’-deoxy-2’-O-methyluridine
|
Others | Others |
Nucleoside Derivatives - Azido-nucleosides, 5’-Modified nucleosides, 2’-Modified nucleosides | |||
TNU1155 |
5’-Azido-5’-deoxy-2’-O-methyl-5-methyluridine
|
Others | Others |
Nucleoside Derivatives - 5’-Modified nucleosides, Azido-nucleosides, 2’-Modified nucleosides | |||
T83813 |
8-Azidoadenosine-5'-O-diphosphate sodium
8-azido-ADP,Click Tag™ 8-Azidoadenosine-5'-O-diphosphate |
||
8-Azidoadenosine-5'-O-diphosphate(8-azido-ADP)是ATP前体和嘌呤受体配体ADP的可点击形式。8-azido-ADP的放射性标记形式已被用作各种蛋白质的光亲和标签,包括从牛脑中分离的谷氨酸脱氢酶(GDH)同工酶,以及从兔网织红细胞中分离的真核翻译起始因子2(eIF2)和鸟苷核苷酸交换因子(GEF)。 | |||
TNU0194 |
3’-Azido-3’-deoxy-5-fluorouridine
|
Others | Others |
Nucleoside Derivatives - Azido-nucleosides, 3’-Modified nucleosides, 5-Modified pyrimidine nucleosides; Fluoro-modified nucleosides | |||
T2096 |
Framycetin sulfate
Neomycin Sulphate B,硫酸新霉素B,Framycetin sulphate |
Antibacterial; Antibiotic | Microbiology/Virology |
Framycetin sulfate (Neomycin Sulphate B) 是一种氨基糖苷类抗生素,是 RNase P 裂解活性抑制剂,Ki 为 35 μM。它抑制锤头状核酶,Ki 值为 13.5 μM,可用于肝性脑病和肠致病性大肠杆菌感染的研究。 | |||
TNU0146 |
3’-Azido-3’-deoxy-5-methyuridine
|
Others | Others |
3'-Azido-3'-deoxy-5-methyuridine is a Azido-nucleoside; 3'-N-Modified nucleoside. | |||
TNU0966 |
2’-Azido-2’-deoxy-5-methyluridine
|
Others | Others |
2'-Azido-2'-deoxy-5-methyluridine is a Nucleoside Derivative - Azido-nucleoside, 2'-Modified nucleoside, 5-Modified pyrimidine nucleoside. | |||
TNU0196 |
3’-Azido-3’-deoxy-5-methoxyuridine
|
Others | Others |
Nucleoside Derivatives - Azido-nucleosides, 5-Modified pyrimidine nucleosides, 3’-Modified nucleosides | |||
TNU0132 |
3’-Azido-3’-deoxy-5-iodouridine
|
Others | Others |
Nucleoside Derivatives –Azido-nucleosides, Halo-nucleosides, 3’-Modified nucleosides, 5-Modified pyrimidine nucleosides; Scaffolds and Templates | |||
TNU0258 |
2’-Azido-2’-deoxy-5-methylcytidine
|
Others | Others |
Nucleoside Derivatives - Azido nucleosides, 5-Modified pyrimidine nucleosides, 2’-Modified nucleosides | |||
TNU0195 |
3’-Azido-3’-deoxy-5-trifluoromethyluridine
|
Others | Others |
Nucleoside Derivatives - Azido-nucleosides, 5-Modified pyrimidine nucleosides, 3’-Modified nucleosides; Fluoro-modified nucleosides | |||
TNU1164 |
5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)-5-methyluridine
|
Others | Others |
5'-Azido-5'-deoxy-2'-O-(2-methoxyethyl)-5-methyluridine is a Nucleoside Derivative - 5'-Modified nucleoside; Azido-nucleoside; 2'-Modified nucleoside. | |||
TNU1250 |
5’-Azido-5’-deoxy-2’-O,4’-C-methyleneuridine
|
Others | Others |
Nucleoside Derivatives - LNA-related nucleosides; 5’-Modified nucleosides; Azido-nucleosides | |||
TNU1302 |
3’-Azido-2’,3’-dideoxy-5-hydroxyuridine
|
Others | Others |
Nucleoside Derivatives - 5-Modified pyrimidine nucleosides; Azido-nucleosides; 2’,3’-Dideoxy nucleosides; Drugs and Inhibitors; Antiviral agent | |||
TNU1161 |
5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)uridine
|
Others | Others |
5'-Azido-5'-deoxy-2'-O-(2-methoxyethyl)uridine is a Nucleoside Derivative - 5'-Modified nucleoside; Azido-nucleoside; 2'-Modified nucleoside. | |||
TNU1143 |
3’-Azido-5’-O-trityl-2’,3’-dideoxy-5-methyluridine
|
Others | Others |
Nucleoside Derivatives - Azido-nucleosides; Drugs and Inhibitors; Zidovudine impurity Q | |||
TNU1204 |
3’-Azido-2’,3’-dideoxyuridine 5’-phosphate diammonium salt
|
Others | Others |
Nucleoside Derivatives - Phosphorus-containing nucleotides, Azido-nucleosides, 2’,3’-Dideoxy-nucleosides | |||
TNU0349 |
3’-Azido-3’-deoxy-5-methyl-beta-L-cytidine
|
Others | Others |
3'-Azido-3'-deoxy-5-methyl-beta-L-cytidine is a Nucleoside Derivative - L-nucleoside, Azido-nucleoside. | |||
TNU0976 |
3’,5’-Di-O-acetyl-2’-azido-2’-deoxy-5-methyluridine
|
Others | Others |
3',5'-Di-O-acetyl-2'-azido-2'-deoxy-5-methyluridine is a Nucleoside Derivative - Azido-nucleoside, 2'-Modified nucleoside, 5-Modified pyrimidine nucleoside. | |||
TNU0838 |
3’-Azido-3’-deoxy-5-nitro-4-deoxyuridine
|
Others | Others |
Nucleosides and Reagents - Azido-nuleoside; Pyridine nucleoside; 3’-N-Modified nucleoside | |||
TNU0350 |
3’-Azido-3’-deoxy-5-fluoro-beta-L-cytidine
|
Others | Others |
3'-Azido-3'-deoxy-5-fluoro-beta-L-cytidine is a Nucleoside Derivative - L-nucleoside, Azido-nucleoside, Fluoro-modified nucleoside, 5-Modified pyrimidine nucleoside. | |||
TNU0967 |
2’-Azido-2’-deoxy-5’-O-(4,4’-dimethoxytrityl)-5-methyluridine
|
Others | Others |
Nucleoside Derivatives - Azido-nucleosides, 2’-Modified nucleosides, 5-Modified pyrimidine nucleosides; Protected nucleosides with NH2/OH group | |||
TNU0347 |
3’-Azido-3’-deoxy-5-fluoro-beta-L-uridine
|
Others | Others |
3'-Azido-3'-deoxy-5-fluoro-beta-L-uridine is a Nucleoside Derivative - L-nucleoside, Azido-nucleoside, Fluoro-modified nucleoside, 5-Modified pyrimidine nucleoside. | |||
TNU0346 |
3’-Azido-3’-deoxy-5-methyl-beta-L-uridine
|
Others | Others |
3'-Azido-3'-deoxy-5-methyl-beta-L-uridine is a Nucleoside Derivative - L-nucleoside, Azido-nucleoside. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-05308 |
CD45 Protein, Human, Recombinant (aa 1-529, His)
GP180,B220,L-CA,protein tyrosine phosphatase, receptor type,... |
Human | HEK293 Cells |
CD45 Protein, Human, Recombinant (aa 1-529, His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 57.4 kDa and the accession number is P08575-5. | |||
TMPY-05387 |
SLAMF7 Protein, Human, Recombinant (hFc)
SLAM family member 7,19A,SLAM7,CS1,CD319,CRACC |
Human | HEK293 Cells |
SLAMF7 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 49.1 kDa and the accession number is Q9NQ25-5. | |||
TMPY-04318 |
GRIK2 Protein, Human, Recombinant (hFc)
GLUR6,EAA4,MRT6,GLR6,glutamate receptor, ionotropic, kainate... |
Human | HEK293 Cells |
GRIK2 (Glutamate Ionotropic Receptor Kainate Type Subunit 2, also known as GluR6) is a Protein Coding gene. The GRIK2 (one of the kainate receptors) gene resides in a genetic linkage region (6q21) associated with bipolar disorder (BPD). The gene coding for GRIK2 has been suggested as a candidate gene for autism based on its localization in the autism-specific region on chromosome 6q21 and the involvement of receptor protein in cognitive functions like learning and memory. GRIK2 belongs to the gl... | |||
TMPY-05547 |
SLAMF7 Protein, Human, Recombinant (hFc), Biotinylated
CS1,SLAM7,CD319,SLAM family member 7,CRACC,19A |
Human | HEK293 Cells |
SLAMF7 Protein, Human, Recombinant (hFc), Biotinylated is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 49.1 kDa and the accession number is Q9NQ25-5. | |||
TMPY-05498 |
SR-BI/SCARB1 Protein, Human, Recombinant (hFc)
HDLQTL6,SR-BI,SRB1,CD36L1,CLA-1,CLA1,scavenger receptor clas... |
Human | HEK293 Cells |
SR-BI/SCARB1 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 73.4 kDa and the accession number is Q8WTV0-5. | |||
TMPJ-00854 |
ETS1 Protein, Human, Recombinant (His)
V-ets Erythroblastosis Virus E26 Oncogene Homolog 1 (Avian),... |
Human | E. coli |
ETS1 Protein (ETS1) is a nuclear protein that belongs to the ETS family. Members of this family recognize the core consensus DNA sequence GGAA/T in target genes. Proteins function either as transcriptional activators or repressors of numerous genes. They are involved in stem cell development, cell senescence and death, and tumorigenesis. ETS1 is a transcription factor, containing one ETS DNA-binding domain and one PNT (pointed) domain. it has been shown to interact with TTRAP, UBE2I and Death As... | |||
TMPK-01357 |
SIRP alpha V5 Protein, Human, Recombinant (His & Avi)
MFR,PTPNS1,P84,BIT,MYD-1,MYD1,SHPS-1,SIRPA,SIRP α,SIRP α V |
Human | HEK293 Cells |
Signal regulatory protein α (SIRPα) is a regulatory membrane glycoprotein from SIRP family expressed mainly by myeloid cells and also by stem cells or neurons.SIRPα acts as inhibitory receptor and interacts with a broadly expressed transmembrane protein CD47 also called the "don´t eat me" signal. | |||
TMPK-01363 |
SIRP alpha V5 Protein, Human, Recombinant (His & Avi), Biotinylated
SIRP alpha,MFR,PTPNS1,SIRP α V5,P84,SHPS-1,BIT,CD17... |
Human | HEK293 Cells |
Signal regulatory protein α (SIRPα) is a regulatory membrane glycoprotein from SIRP family expressed mainly by myeloid cells and also by stem cells or neurons.SIRPα acts as inhibitory receptor and interacts with a broadly expressed transmembrane protein CD47 also called the "don´t eat me" signal.Cancer cells highly expressed CD47 that activate SIRP α and inhibit macrophage-mediated destruction. SIRP alpha V5 Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian c... |