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17
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10964 |
DB1976
|
Apoptosis; Others | Apoptosis; Others |
DB1976 是一种 DB270 的硒烯类似物,是一种高效且可渗透细胞的转录因子 PU.1 的抑制剂。在体外,DB1976 有效抑制 PU.1 结合 (IC50 为 10 nM),可强烈抑制 PU.1/DNA 复合物 (具有高 DB1976-λB 亲和力,KD 为 12 nM)。DB1976 具有诱导细胞凋亡的作用。 | |||
T3200 |
DB07268
|
JNK | MAPK |
DB07268 是选择性JNK1抑制剂,IC50值为 9 nM。 | |||
T64372 |
DB722
|
Others | Others |
DB722是一种具有DNA 结合活性的呋喃脒类似物。DB722显示抗增殖活性。 | |||
T9707 |
DB2313
Carboximidamide |
Apoptosis | Apoptosis |
DB2313 (Carboximidamide) 是一种有效的转录因子 PU.1 抑制剂,IC50 为 14 nM。DB2313 破坏了 PU.1 与靶基因启动子的相互作用。DB2313 可诱导急性髓细胞性白血病 (AML) 细胞凋亡 (apoptosis),并具有抗癌作用。 | |||
T15055 |
DB04760
MMP-13 Inhibitor |
MMP | Proteases/Proteasome |
DB04760 是一种高选择性和有效的 MMP-13 非锌螯合抑制剂(IC50:8 nM)。DB04760 能明显降低紫杉醇的神经毒性,并具有抗癌活性。 | |||
T24421 |
LY-2624803
DB-7,LY2624803,HY-10275,LY 2624803 |
5-HT Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
LY-2624803 是一种 5-HT2A 受体拮抗剂和组胺受体反向激动剂,可用于改善慢波睡眠。 | |||
T27124 |
DB-959 (salt)
T3D959,T-3D-959,T-3D959,DB-959Na,DB959Na |
||
DB-959, a PPAR agonist, is used potentially for the treatment of Alzheimer's disease. | |||
Fr13634 |
4-Aminobenzamide
红色基DB-70 |
||
Compound Fr13634 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 Fr13634,CAS号为 2835-68-9。 | |||
T31215 |
DB-766
DB766 |
||
DB-766 is a potential chemotherapeutic candidate for Chagas' disease treatment. DB-766 exhibits strong trypanocidal activity and excellent selectivity for bloodstream trypomastigotes and intracellular amastigotes (Y strain), giving IC(50)s of 60 and 25 nM | |||
T69674 |
DB-310
|
||
DB-310 is a novel LMP2 inhibitor as a potential treatment for Alzheimer's disease. | |||
T23967 | DB-959 (free base) | ||
DB-959 is a potential agonist of PPAR. | |||
T31425 |
Dibenz[a,h]anthracene
CCRIS 208,二苯葸,NSC 22433,AI3-18996,DB(a,h)A |
DNA | DNA Damage/DNA Repair |
Dibenz[a,h]anthracene (CCRIS 208) 诱导细菌DNA 损伤和基因突变,并在几种哺乳动物细胞培养物中诱导基因突变和转化。 | |||
T23966 |
DB772
DB 772,DB-772 |
||
DB772 is a scrapie prion accumulation inhibitor. | |||
T24587 |
Pafuramidine maleate
DB-289,DB289,DB 289 |
||
Pafuramidine is an orally bioavailable prodrug of formamidine which was developed for the treatment of human African trypanosomiasis. | |||
T77925 |
DB-0646
|
PROTACs | PROTAC |
DB-0646是一种靶向蛋白降解剂(PROTAC),具有多激酶抑制特性。 | |||
T26003 |
Pyrazinobutazone
DB139,Carudol,DB-139,Ranoroc,DB 139 |
||
Pyrazinobutazone is an antipyrene derivative which possesses anti-inflammatory properties. | |||
T68487 |
DB1055
|
||
DB1055 is a novel HOXA9 Transcription Factor Inhibitor, dedemonstrating for the first time the propensity of sequence-selective DNA ligands to inhibit HOXA9/DNA binding. | |||
T74101 | DB-3-291 | ||
DB-3-291 是一种有效和选择性的CSK 降解剂,Kd 值为 1 nM。 | |||
T68359 |
DB1255
|
||
DB1255 is a ERG/DNA binding inhibitor which targets the DNA-binding activity of the human ERG transcription factor. | |||
T9958 | DB818 | Others | Others |
DB818 是一种合成的 Homeobox A9 (HOXA9) 抑制剂,可用于治疗与 HOXA9 过表达相关的急性髓细胞白血病。 | |||
T31891 |
Furidarone
DB 136,Furidarona,Furidaronum |
||
Furidarone is a biochemical. | |||
T23898 |
Clocoumarol
Clocoumarolum,BRN 1264788,DB 112 |
||
Clocoumarol is an anticoagulant that prevents blood clotting. It also can inhibit the dilatation of the spleen and the congestion of lymph nodes. | |||
T10964L |
DB1976 dihydrochloride
DB1976 hydrochloride,DB1976 2HCl |
Apoptosis; NF-κB | Apoptosis; NF-κB |
DB1976 dihydrochloride (DB1976 2HCl) ,一种转录因子 PU.1 抑制剂,具有潜在抗炎活性,可在体内实验中减缓小鼠的炎症和纤维化,改善了葡萄糖稳态和血脂异常。DB1976 dihydrochloride 促进细胞凋亡,可用于研究代谢功能障碍和非酒精性脂肪性肝炎。 | |||
T38778 |
DB2115 tertahydrochloride
DB2115 tertahydrochloride |
||
DB2115 (tertahydrochloride) is a powerful inhibitor of the myeloid master regulator PU.1. With significant potential in cancer research, particularly hematologic cancers like leukemia, as well as other conditions linked to PU.1 dysfunction, DB2115 (tertahydrochloride) offers promising avenues of study. | |||
T71585 | DB03417 | ||
DB03417 is a compound listed in web page: https://go.drugbank.com/drugs/DB03417. DB03417 is a potential tryptase inhibitor. | |||
T69857 |
DB293
|
||
DB293 is an inhibitor of PIT-1 and BRN-3 transcription factors. DB293 binds as head-to-tail stacked dimers in the minor groove of 5'-ATGA sequence, thereby leading to an increase in the size of minor groove. | |||
T24414 |
Lofepramine hydrochloride
WHR-2908A,DB-2182,WHR 2908A |
||
Lofepramine is a serotonin and norepinephrine reuptake inhibitor. Lofepramine is also a psychotropic IMIPRAMINE derivative. | |||
T23994 |
Dibenzo(a,i)pyrene
DB(a,i)p,Benzo(rst)pentaphene |
||
Dibenzo(a, i)pyrene is a polycyclic aromatic hydrocarbon with potent carcinogenic activity. | |||
T27395 |
Furamidine dihydrochloride
DB 75, DB75, NSC 305831, WR199385,Furamidine HCl |
||
Furamidine is a cell-permeable, selective inhibitor of protein arginine methyltransferase 1 (PRMT1). Furamidine binds to strings of AT base pair sequences in DNA′s minor groove. Furamidine targets the enzyme active site and is primarily competitive with t | |||
T2330 |
Rilpivirine
TMC278,R278474,利匹韦林,DB08864 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Rilpivirine (R278474) 是一种二芳基嘧啶衍生物和非核苷逆转录酶抑制剂,具有抗 HIV-1 的抗病毒活性,用于治疗 HIV 感染。 | |||
T32737 |
Liafensine
BMS820836,BMS 820836,DB104,BMS-820836 |
Dopamine Receptor; 5-HT Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Liafensine(BMS-820836) 是一种新型且具有选择性的三重单胺再摄取抑制剂,对血清素、去甲肾上腺素和多巴胺的再摄取具有抑制作用,可用于研究重度抑郁症和中枢神经系统疾病。 | |||
T15056 | DB07107 | Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
DB07107 is a potent inhibitor of drug resistant T315I mutant Bcr-Abl tyrosine kinase and a potent Akt1 inhibitor (IC50: 360 nM). | |||
T16428 |
Pafuramidine
DB289 |
Others | Others |
Pafuramidine is an orally bioavailable prodrug of furamidine. It has activity against Pneumocystis pneumonia (IC50 value: 4.5 nM) | |||
T71583 | Amlodipine hydrochloride, (R)- | ||
Amlodipine hydrochloride, (R)-, is a medication used to lower blood pressure and prevent chest pain. It belongs to a group of medications known as dihydropyridine-type calcium channel blockers. By widening of blood vessels it lowers blood pressure. In angina, amlodipine increases blood flow to the heart muscle to relieve pain due to angina. | |||
T69841 | GC813 sodium | ||
GC813 is a potent and permeable inhibitor of MERS coronavirus 3CL protease. GC813 is analogue of GC376. | |||
T69856 |
Pralurbactam
|
||
Pralurbactam 是 β -内酰胺酶抑制剂。Pralurbactam 可用于细菌感染的研究。 | |||
T69673 |
Deucrictibant
|
||
Deucrictibant is a bradykinin receptor antagonist. | |||
T11338 |
Furamidine
DB75,NSC 305831 |
Others | Others |
Furamidine is also a selective and cell-permeable protein arginine methyltransferase 1 (PRMT1) inhibitor with an IC50 of 9.4 μM. Furamidine is selective for PRMT1 over PRMT5, PRMT6, and PRMT4 (CARM1) (IC50s of 166 μM, 283 μM, and >400 μM, respectively). Furamidine (DB75) is abisbenzamidine derivative and an antiparasite agent. Furamidine is a potent, reversible and competitive tyrosyl-DNA phosphodiesterase 1 (TDP-1) inhibitor. Inhibition of TDP-1 by Furamidine is effective both with single- and ... | |||
T19272 |
DB04760 analog 1
|
Others | Others |
DB04760 analog 1 is an analogue of DB04760. | |||
T74642 |
DB1113
|
||
DB1113 (Example 24) 是一种靶向蛋白激酶降解的双功能化合物。DB1113 可降解 ABL1,ABL2,BLK,CDK11B,CDK4,CSK,EPHA3,FER,GAK,LIMK1,MAP3K20,MAP4K1,MAP4K2,MAP4K3,MAP4K5,MAPK14,MAPK7,MAPK8,MAPK9,MAPKAPK2,MAPKAPK3,NLK,PDIK1L,PTK2B,RIPK1,RPS6KA1,RPS6KA3,SIK2,SIK3,STK35,TNK2 和 ULK1。DB1113 可用于研究异常激酶活性介导的疾病或紊乱。 | |||
T73542 | DB008 | ||
DB008 是一种有效的选择性PARP16抑制剂,IC50值为 0.27 μM,含有丙烯酰胺亲电试剂。DB008 具有膜渗透性,可选择性标记PARP16。 | |||
T74644 |
DB0614
|
||
DB1113 (Example 24) 是一种靶向蛋白激酶降解的双功能化合物。DB1113 可降解ABL1,ABL2,BLK,CDK11B,CDK4,CSK,EPHA3,FER,GAK,LIMK1,MAP3K20,MAP4K1,MAP4K2,MAP4K3,MAP4K5,MAPK14,MAPK7,MAPK8,MAPK9,MAPKAPK2,MAPKAPK3,NLK,PDIK1L,PTK2B,RIPK1,RPS6KA1,RPS6KA3,SIK2,SIK3,STK35,TNK2 和ULK1。DB1113 可用于研究异常激酶活性介导的疾病或紊乱。 | |||
T69842 |
DB2313 HCl
|
||
DB2313 is a first-in-class potent small-molecule inhibitor of PU.1. DB2313 disrupts the interaction of PU.1 with target gene promoters and leads to down-regulation of canonical PU.1 transcriptional targets. | |||
T63412 | DB772 hydrate | ||
DB772 hydrate 是一种牛病毒性腹泻病毒 (BVDV) 抑制剂,同时表现出抗朊病毒作用。 | |||
T69354 |
Enzastaurin 2HCl
|
||
Enzastaurin 2HCl, also known as DB-102 and LY317615, is a synthetic macrocyclic bisindolemaleimide with potential antineoplastic activity. Binding to the ATP-binding site, Enzastaurin 2HCl selectively inhibits protein kinase C beta, an enzyme involved in the induction of vascular endothelial growth factor (VEGF)-stimulated neo-angiogenesis. This agent may decrease tumor blood supply and so tumor burden. | |||
T71853 |
Enzastaurin HCl
|
||
Enzastaurin HCl, also known as DB-102 and LY317615, is a synthetic macrocyclic bisindolemaleimide with potential antineoplastic activity. Binding to the ATP-binding site, Enzastaurin HCl selectively inhibits protein kinase C beta, an enzyme involved in the induction of vascular endothelial growth factor (VEGF)-stimulated neo-angiogenesis. This agent may decrease tumor blood supply and so tumor burden. | |||
T82605 |
DB21, Galectin-1 Antagonist
|
Galectin | Immunology/Inflammation |
DB21, Galectin-1 Antagonist 是一种用于抑制galectin-1 (GAL1)与细胞表面聚糖结合的二苯并呋喃缀合肽模拟物。在黑色素瘤、肺腺癌和卵巢癌模型中,该化合物能增强血管生成和肿瘤生长的抑制效果。 | |||
T27933 |
LY243246
LY249543 disodium,LY249543 sodium,LY 249543,LY-249543,S-isomer of lometrexol,DB04322,LY249543 |
||
LY249543, the S-isomer of lometrexol, is an inhibitor of Methylenetetrahydrofolate Dehydrogenase/Cycl. | |||
T15073 |
DBCO-PEG4-NHS ester
|
PROTAC Linker | PROTAC |
DBCO-PEG4-NHS ester 是一种属于 PEG 类的 PROTAC linker,可用于 PROTAC 分子的合成。 | |||
T15067 |
DBCO-NHS ester
|
Others | Others |
DBCO-NHS ester 是一种 ADC 连接剂,可裂解的 3 单元 PEG,还可以用于合成抗体药物共轭物 (ADC)。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN3484 | Bakkenolide Db | Others | Others |
Bakkenolide Db may have cytotoxicity. | |||
T80779 |
WDB002
|
||
WDB002,一种FK506/雷帕霉素家族的天然产物,靶向CEP250,可应用于COVID-19研究。 | |||
T3414 |
Morroniside
莫诺苷,奎宁树 |
Apoptosis; MMP; Pyroptosis | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Morroniside 通过抑制神经元凋亡和 MMP9/2 的表达从而发挥神经保护作用,可作为 db/db 小鼠肝脏炎症反应和脂质代谢的调节剂。它通过抑制高血糖和氧化应激表现出对糖尿病肾损伤和人脐静脉内皮细胞的保护作用。 | |||
TN3532 | Borapetoside E | Others | Others |
Borapetoside E has anti-hyperglycemic activity, it can significantly reduce serum glucose levels at dose-dependent manners in alloxan-induced hyperglycemic mice and db/db type 2 diabetic mice. | |||
T5706 |
8-epidiosbulbin E acetate
|
Others | Others |
8-epidiosbulbin E acetate 是亚洲国家广泛使用的传统草药 Dioscorea bulbifera L. (DB) 中含量丰富的二萜内酯。 | |||
T38250 | L-Sepiapterin | ||
L-Sepiapterin, also known as Sepiapterin, is a precursor compound crucial for the production of tetrahydrobiopterin (BH4), which serves as a coenzyme for endothelial nitric oxide synthase (eNOS). This compound demonstrates its efficacy by improving endothelial dysfunction in small mesenteric arteries from db/db mice and promoting angiogenesis. Moreover, L-Sepiapterin exerts inhibitory effects on cellular proliferation and migration in ovarian cancer cells through the down-regulation of p70S6K-de... | |||
TN3779 | De-O-methyllasiodiplodin | IL Receptor; TNF; ROS; Antifection | Apoptosis; Immunology/Inflammation; Microbiology/Virology |
De-O-methyllasiodiplodin exhibits radical scavenging, moderate antibacterial, and potential anti-inflammatory effects, it shows moderate suppression effects on induced NO production. De-O-methyllasiodiplodin effectively lowers the blood glucose level in d |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPJ-00411 |
LEPR Protein, Human, Recombinant (hFc)
LEPR,Leptin receptor,OB-R,OB receptor,OBR,CD295,DB,... |
Human | Human Cells |
The Leptin receptor is a member of the Class I cytokine receptor family. It mediates the activities of Leptin, a multi-functional hormone produced primarily by adipose tissues that plays roles in food intake, energy metabolism, angiogenesis, reproduction, hematopoiesis, bone metabolism, and immune function. The human Leptin R gene encodes 1165 amino acids (aa) including a signal peptide, an extracellular region with cytokine receptor homology (CRH), multiple fibronectin type III domains and a WS... | |||
TMPJ-00976 |
LEPR Protein, Mouse, Recombinant (His)
OBR,DB,Leptin receptor,OB receptor,CD295,OB-R,LEPR,... |
Mouse | Human Cells |
The Leptin receptor is a member of the Class I cytokine receptor family. It mediates the activities of Leptin, a multi-functional hormone produced primarily by adipose tissues that plays roles in food intake, energy metabolism, angiogenesis, reproduction, hematopoiesis, bone metabolism, and immune function. The human Leptin R gene encodes 1165 amino acids (aa) including a signal peptide, an extracellular region with cytokine receptor homology (CRH), multiple fibronectin type III domains and a WS... | |||
TMPJ-00977 |
LEPR Protein, Mouse, Recombinant (mFc)
LEPR,CD295,OB-R,LEP-R,HuB219,Leptin receptor,OBR,DB... |
Mouse | Human Cells |
The Leptin receptor is a member of the Class I cytokine receptor family. It mediates the activities of Leptin, a multi-functional hormone produced primarily by adipose tissues that plays roles in food intake, energy metabolism, angiogenesis, reproduction, hematopoiesis, bone metabolism, and immune function. The human Leptin R gene encodes 1165 amino acids (aa) including a signal peptide, an extracellular region with cytokine receptor homology (CRH), multiple fibronectin type III domains and a WS... | |||
TMPJ-00975 |
LEPR Protein, Mouse, Recombinant (hFc)
CD295,DB,HuB219,OB receptor,LEP-R,Leptin receptor,O... |
Mouse | Human Cells |
The Leptin receptor is a member of the Class I cytokine receptor family. It mediates the activities of Leptin, a multi-functional hormone produced primarily by adipose tissues that plays roles in food intake, energy metabolism, angiogenesis, reproduction, hematopoiesis, bone metabolism, and immune function. The human Leptin R gene encodes 1165 amino acids (aa) including a signal peptide, an extracellular region with cytokine receptor homology (CRH), multiple fibronectin type III domains and a WS... | |||
TMPH-02492 |
DBI Protein, Mouse, Recombinant (His & Myc)
Endozepine (EP),Diazepam-binding inhibitor,DBI,Acyl... |
Mouse | E. coli |
Binds medium- and long-chain acyl-CoA esters with very high affinity and may function as an intracellular carrier of acyl-CoA esters. It is also able to displace diazepam from the benzodiazepine (BZD) recognition site located on the GABA type A receptor. It is therefore possible that this protein also acts as a neuropeptide to modulate the action of the GABA receptor. | |||
TMPH-02972 |
VDB Protein, Mouse, Recombinant (E. coli, His)
|
Mouse | E. coli |
Involved in vitamin D transport and storage, scavenging of extracellular G-actin, enhancement of the chemotactic activity of C5 alpha for neutrophils in inflammation and macrophage activation. | |||
TMPH-03561 |
lsdB Protein, S. aureus, Recombinant (His & SUMO)
|
Staphylococcus aureus | E. coli |
Cell wall-anchored surface receptor that extracts heme from oxidized metHb to enable growth on hemoglobin as a sole iron source. Rapidly extracts heme from hemoglobin and transfers it to IsdA or IsdC, which then relays it to the membrane transporter/IsdEF for internalization. Promotes also resistance to hydrogen peroxide and killing by neutrophils. | |||
TMPY-05552 |
DBT Protein, Human, Recombinant (His)
E2,BCKAD-E2,BCKADE2,DBT,BCATE2,RP11-35E17.3,E2B |
Human | Baculovirus-Insect Cells |
DBT Protein, Human, Recombinant (His) is expressed in Baculovirus-Insect Cells with His tag. The predicted molecular weight is 48.8 kDa. Accession number: P11182 | |||
TMPY-03991 |
DBI Protein, Human, Recombinant (His)
diazepam binding inhibitor (GABA receptor modulator, acyl-Co... |
Human | E. coli |
The diazepam binding inhibitor (DBI), alternatively known as the acyl-CoA binding protein (ACBP), is involved in multiple biological actions. The polypeptide binds to the peripheral, or mitochondrial, benzodiazepine receptor and facilitates transport of cholesterol to the inner membrane to stimulate steroid synthesis. Through this action, DBI indirectly modulates gamma-aminobutyric acid (GABA)-mediated inhibitory neurotransmission. DBI can be postulated as a candidate gene for psychiatric phenot... | |||
TMPH-02973 |
VDB Protein, Mouse, Recombinant (His)
|
Mouse | Yeast |
Involved in vitamin D transport and storage, scavenging of extracellular G-actin, enhancement of the chemotactic activity of C5 alpha for neutrophils in inflammation and macrophage activation. | |||
TMPH-00890 |
DBI Protein, Human, Recombinant (aa 2-104, His)
Acyl-CoA-binding protein,Diazepam-binding inhibitor,DB |
Human | E. coli |
Binds medium- and long-chain acyl-CoA esters with very high affinity and may function as an intracellular carrier of acyl-CoA esters. It is also able to displace diazepam from the benzodiazepine (BZD) recognition site located on the GABA type A receptor. It is therefore possible that this protein also acts as a neuropeptide to modulate the action of the GABA receptor. | |||
TMPH-02178 |
TARDBP Protein, Human, Recombinant
|
Human | E. coli |
RNA-binding protein that is involved in various steps of RNA biogenesis and processing. Preferentially binds, via its two RNA recognition motifs RRM1 and RRM2, to GU-repeats on RNA molecules predominantly localized within long introns and in the 3'UTR of mRNAs. In turn, regulates the splicing of many non-coding and protein-coding RNAs including proteins involved in neuronal survival, as well as mRNAs that encode proteins relevant for neurodegenerative diseases. Plays a role in maintaining mitoch... | |||
TMPJ-00759 |
VDB Protein, Human, Recombinant (His)
Group-Specific Component,DBP,VDB,GC,Gc-Glo... |
Human | Human Cells |
Vitamin D-Binding Protein (DBP) is a member of the ALB/AFP/VDB family. DBP is a secreted protein and contains three albumin domains. The primary structure contains 28 cysteine residues forming multiple disulfide bonds. DBP acts as a multifunctional protein found in plasma, ascitic fluid, cerebrospinal fluid, and urine and on the surface of many cell types. DBP binds to vitamin D and its plasma metabolites and transports them to target tissues. DBP associates with membrane-bound immunoglobulin on... | |||
TMPH-02179 |
TARDBP Protein, Human, Recombinant (His)
|
Human | Yeast |
RNA-binding protein that is involved in various steps of RNA biogenesis and processing. Preferentially binds, via its two RNA recognition motifs RRM1 and RRM2, to GU-repeats on RNA molecules predominantly localized within long introns and in the 3'UTR of mRNAs. In turn, regulates the splicing of many non-coding and protein-coding RNAs including proteins involved in neuronal survival, as well as mRNAs that encode proteins relevant for neurodegenerative diseases. Plays a role in maintaining mitoch... | |||
TMPH-03235 |
DBI Protein, Rat, Recombinant (His & Myc)
Endozepine (EP),ACBP,DBI,Acyl-CoA-binding protein,D... |
Rat | E. coli |
Binds medium- and long-chain acyl-CoA esters with very high affinity and may function as an intracellular carrier of acyl-CoA esters. It is also able to displace diazepam from the benzodiazepine (BZD) recognition site located on the GABA type A receptor. It is therefore possible that this protein also acts as a neuropeptide to modulate the action of the GABA receptor. | |||
TMPK-00839 |
ITGB6 Protein, Human, Recombinant (His)
β6,Integrin β-6,β 6,beta 6,Integrin β 6,Integrin beta-6,Inte... |
Human | HEK293 |
ITGB6 is known to be one of the major receptor components involved in host tropism of foot-and-mouth disease (FMD) virus in cattle. A competitive PCR technique called ARMS PCR was adapted to identify a single-nucleotide polymorphism (SNP), G29A, db SNP Id: rs109075046, in the 5' untranslated region (5'UTR) of the bovine ITGB6 gene. | |||
TMPK-01247 |
ITGB6 Protein, Mouse, Recombinant (His)
ITGB6,Integrin β-6,Integrin beta-6 |
Mouse | HEK293 |
ITGB6 is known to be one of the major receptor components involved in host tropism of foot-and-mouth disease (FMD) virus in cattle. A competitive PCR technique called ARMS PCR was adapted to identify a single-nucleotide polymorphism (SNP), G29A, db SNP Id: rs109075046, in the 5' untranslated region (5'UTR) of the bovine ITGB6 gene. |