73
14
8
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7391 |
SAR407899
|
ROCK; Rho | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
SAR407899 是一种选择性的 ATP 竞争性ROCK 抑制剂,对ROCK-2的IC50值为 135 nM,对人和大鼠ROCK-2的Ki 值分别为 36 和 41 nM。它是 Rho 激酶抑制剂,有效抑制 endothelin-1 诱导的肾阻力动脉收缩。 | |||
T2155 |
Thiazovivin
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Thiazovivin 是一种ROCK 抑制剂,能提高 iPSC 的生成效率,对人胚胎干细胞具有保护作用。 | |||
T7301 |
BDP5290
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
BDP5290 是一种有效 ROCK 和 MRCK 抑制剂,对 ROCK1、ROCK2、MRCKα 和 MRCKβ 的 IC50 分别为 5、50 、10 和 100 nM。 | |||
T12746 |
ROCK inhibitor-2
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
ROCK inhibitor-2 是一种 ROCK1和 ROCK2的选择性双重抑制剂,IC50值分别为 17 nM 和2 nM。 | |||
T3513 |
GSK180736A
GSK180736 |
ROCK; GRK; PKA | Cell Cycle/Checkpoint; Cytoskeletal Signaling; GPCR/G Protein; Stem Cells; Tyrosine Kinase/Adaptors |
GSK180736A 是 Rho 相关卷曲螺旋激酶 1 (ROCK1) 抑制剂,IC50值为 100 nM。它也是选择性的ATP-竞争性 G 蛋白偶联受体激酶 2 抑制剂,IC50值为 0.77 μM,其选择性比其他 GRK 高 100 倍以上。 | |||
T4095 |
ZINC00881524
ROCK inhibitor |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
ZINC00881524 (ROCK inhibitor)是一种特异性有效 ROCK 抑制剂。 | |||
T15798 |
LX7101
|
ROCK; LIM Kinase; PKA | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells; Tyrosine Kinase/Adaptors |
LX7101是 LIMK 和ROCK2高效抑制剂,对LIMK1/2、ROCK、PKA 的IC50分别为24、1.6、10 和小于1 nM。 | |||
T14989 |
CMPD101
|
ROCK; GRK; PKC | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; GPCR/G Protein; Stem Cells |
CMPD101 是膜透性的 GRK2/3高选择性小分子抑制剂,IC50分别为 18 nM 和 5.4 nM。它针对 GRK1、GRK5 ROCK-2 和 PKCα 的选择性较小,IC50值分别为 3.1 μM,2.3 μM,1.4 μM 和 8.1 μM,可研究心衰疾病。 | |||
T2633 |
GSK429286A
RHO-15 |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
GSK429286A (RHO-15) 是一种选择性ROCK1/2抑制剂,IC50值为14 和 63 nM。 | |||
T14960 |
Chroman 1
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Chroman 1 是高效的的ROCK 选择性抑制剂,对 ROCK2 (IC50=1 pM) 的抑制作用强于 ROCK1 (IC50=52 pM) 。它对MRCK 也有抑制作用,IC50为 150 nM。 | |||
T7885 |
Afuresertib hydrochloride
|
ROCK; Akt; PKC | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Stem Cells |
Afuresertib hydrochloride 是一个口服有效的,ATP 竞争性的选择性泛Akt 抑制剂,作用于Akt1、Akt2和Akt3,Ki 值分别为 0.08、2和 2.6 nM。 | |||
TQ0187 |
SR-3677
|
ROCK; Autophagy | Autophagy; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
SR-3677 是一种有效且特异性的 ROCK2 抑制剂,IC50值为3 nM。 | |||
T12747 |
ROCK2-IN-2
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
ROCK2-IN-2 是 ROCK2 的特异性抑制剂(IC50 <1 μM)。 | |||
T1898 |
RKI-1447
RKI1447 |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
RKI-1447 是一种高效的ROCK1和ROCK2的小分子抑制剂,IC50值分别为14.5和6.2 nM。 | |||
T1870 |
Y-27632
|
ROCK; Apoptosis | Apoptosis; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Y-27632 是一种 ROCK-I 和 ROCK-II 抑制剂,具有口服有效性、ATP 竞争性。Y-27632 还抑制分离诱导的小鼠前列腺干或祖细胞凋亡。 | |||
T4488 |
GSK-25
GSK25 |
ROCK; S6 Kinase; mTOR | Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling; Stem Cells |
GSK-25 是一种选择性的,具有口服活性的 ROCK1抑制剂。它对 31 种激酶以及 RSK1 和 p70S6K 保持良好的选择性,RSK1的 IC50 为 398 nM,p70S6K 的 IC50 为 1000nM。它可抑制 P450,对 CYP2C9、CYP2D6和 CYP3A4的 IC50分别为2.5、5.2和2.5 μM。 | |||
T2011 |
RKI1313
RKI 1313,RKI-1313 |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
RKI1313 (RKI-1313) 是一种选择性抑制剂,可抑制 ROCK 依赖性信号传导、细胞骨架变化、不依赖锚定的集落形成、迁移和侵袭。 | |||
T7648 |
HA-100
|
Myosin; PKA; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
HA-100 是蛋白激酶和ROCK 抑制剂,抑制PKG,PKA,PKC 和MLC 激酶的IC50值分别为 4、8、12 和 240 μM。 | |||
T6867 |
Belumosudil
KD025,Rezurock,ROCK inhibitor,SLx-2119 |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Belumosudil (Rezurock) 是一种选择性的ROCK2抑制剂,对 ROCK1 和 ROCK2 的IC50值分别为 24 µM 和 105 nM,具有抗纤维化作用。 | |||
T23308 |
SAR407899 hydrochloride
6-(哌啶-4-氧基)异喹啉-1(2H)-酮盐酸盐 |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
SAR407899 hydrochloride 是一种选择性,ATP 竞争性的ROCK 抑制剂,对人和大鼠ROCK2的Ki 值分别为 36 和 41 nM,对ROCK2的IC50值为 135 nM。 | |||
T7764 |
CCG-222740
|
ROCK; Rho; Ras | Cell Cycle/Checkpoint; Cytoskeletal Signaling; GPCR/G Protein; MAPK; Stem Cells |
CCG-222740 是一种口服有效的选择性Rho/MRTF 途径抑制剂。它也是 α-平滑肌的肌动蛋白表达抑制剂,可减少皮肤纤维化并阻止黑色素瘤转移。 | |||
T13384L |
Y-33075 dihydrochloride
|
CaMK; ROCK; PKC | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Neuroscience; Stem Cells |
Y-33075 dihydrochloride 是一种选择性ROCK 抑制剂,IC50为 3.6 nM。 | |||
TQ0110 |
ROCK-IN-2
TC-S 7001,Azaindole 1 |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
ROCK-IN-2 (Azaindole 1) 是一种选择性,ATP-竞争型的ROCK 抑制剂,对ROCK-1和ROCK-2的IC50值分别为 0.6 和 1.1 nM。 | |||
T2482 |
AT13148
|
ROCK; SGK; Akt; PKA; S6 Kinase | Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells; Tyrosine Kinase/Adaptors |
AT13148 是一种 ATP 竞争性 AGC 激酶口服抑制剂,能够抑制 Akt1/Akt2/Akt3、p70S6K、PKA 和 ROCKI/ROCKII 的活性,IC50值分别为 38/402/50、8、3 和 6 nM/4 nM。 | |||
T1911 |
Afuresertib
GSK2110183C,GSK2110183 |
ROCK; Akt; PKC | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Stem Cells |
Afuresertib (GSK2110183) 是一个选择性,ATP 竞争性,口服有效的泛 Akt 抑制剂,作用于 Akt1、Akt2和 Akt3,Ki 值分别为 0.08、2、2.6 nM。 | |||
T4276L |
Hydroxyfasudil
Hydroxy-Fasudil,HA-1100,羟基法舒地尔 |
ROCK; PKA | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells; Tyrosine Kinase/Adaptors |
Hydroxyfasudil (Hydroxy-Fasudil) 是一种ROCK 抑制剂,对ROCK1和ROCK2的IC50分别为 0.73 和 0.72 μM。 | |||
T3518 |
GSK269962A
GSK269962B,GSK 269962,GSK269962A HCl |
ROCK; S6 Kinase | Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling; Stem Cells |
GSK269962A (GSK269962A HCl) 是一种有效的ROCK 抑制剂,具有抗炎和血管舒张作用。它作用于重组人ROCK1和ROCK2,IC50分别为 1.6 和 4 nM。 | |||
T4276 |
Hydroxyfasudil Hydrochloride
Hydroxyfasudil (HA-1100) HCl,羟基法舒地尔盐酸盐,RHO-激酶抑制剂,HA 1100 hydrochloride |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Hydroxyfasudil Hydrochloride (HA 1100 hydrochloride) 是一种ROCK 抑制剂,对ROCK1和ROCK2的IC50值分别为 0.73 和 0.72 μM。 | |||
T1725 |
Y-27632 dihydrochloride
反式-4-[(R)-1-氨基乙基]-N-(4-吡啶基)环己烷甲酰胺二盐酸盐,Y-27632 2HCl |
ROCK; Apoptosis | Apoptosis; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Y-27632 dihydrochloride (Y-27632 2HCl) 是一种 ROCK-I 和 ROCK-II 抑制剂,具有口服有效性、ATP 竞争性。Y-27632 dihydrochloride 还抑制分离诱导的小鼠前列腺干或祖细胞凋亡。 | |||
T7552 |
H-1152
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
H-1152 是一种膜通透的选择性ROCK 抑制剂,Ki 为 1.6 nM,对ROCK2的IC50为 12 nM。 | |||
T1606 |
Fasudil
HA-1077,AT877,法舒地尔 |
ROCK; Serine/threonin kinase; Calcium Channel; PKA; PKC; Autophagy | Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Membrane transporter/Ion channel; Metabolism; Stem Cells; Tyrosine Kinase/Adaptors |
Fasudil (HA-1077) 是一种非特异性 RhoA/ROCK 抑制剂,也是 Ca2+通道拮抗剂和血管扩张剂。它对蛋白激酶有抑制作用,ROCK1 的 Ki 值为 0.33 μM,ROCK2 和 PKA、PKC、PKG 的 IC50值分别 0.158 μM 和 4.58 μM、12.30 μM、1.650 μM。 | |||
T7492 |
Ripasudil free base
K-115 (free base) |
ROCK; Antibacterial | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Microbiology/Virology; Stem Cells |
Ripasudil free base (K-115 (free base)) 是一种ROCK 特异性抑制剂,能够抑制ROCK1和ROCK2的活性,IC50值分别为 51 和 19 nM。 | |||
T3060 |
Fasudil hydrochloride
Fasudil (HA-1077) HCl,盐酸法舒地尔,HA-1077,Fasudil HCl,HA-1077 hydrochloride,AT-877 |
ROCK; Serine/threonin kinase; Calcium Channel; HIV Protease; PKA; PKC; Autophagy | Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Proteases/Proteasome; Stem Cells; Tyrosine Kinase/Adaptors |
Fasudil hydrochloride (HA-1077) 是一种非特异性RhoA/ROCK 抑制剂,也抑制蛋白激酶,对 ROCK1、PKA、PKC 和 MLCK 的 Ki 值分别为 0.33 μM、1.0 μM、9.3 μM 和 55 μM。 | |||
TP1008 |
Neurokinin A
α-Neurokinin,Substance K,神经激肽A,Neuromedin L |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Neurokinin A (NKA) 是速激肽家族的一种肽类神经递质,是人体气管道和胃肠道组织中的主要介体,可通过 NK-2受体发挥作用。 | |||
TP1363L |
Neurokinin B acetate(86933-75-7 free base)
神经激肽 B醋酸盐,Neurokinin K |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Neurokinin B acetate(86933-75-7 free base) 是属于速激肽家族的神经激肽 B 的醋酸盐形式。神经激肽与神经激肽受体 1 (NK1R)、nk2r 和 NK3R 结合,并介导其生物学效应。 | |||
T22517 |
5,7-Dichlorokynurenic acid
5,7-二氯犬尿喹啉酸,5,7-dichlorokynurenic acid sodium,5,7-DCKA |
NMDAR | Neuroscience |
5,7-Dichlorokynurenic acid (5,7-dichlorokynurenic acid sodium) 是一种专门针对于NMDA 受体甘氨酸位点的竞争性拮抗剂(KB:65 nM)。它是犬尿酸的衍生物,可降低大鼠皮质细胞培养物中 NMDA 诱导的神经元损伤程度。 | |||
TP1385 |
Neurokinin A(4-10) TFA(97559-35-8 free base)
Neurokinin A(4-10) TFA |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Neurokinin A(4-10) TFA(97559-35-8 free base) 是一种速激肽 NK2 受体激动剂。 | |||
T76429 |
Neurokinin Receptor (393-407), rat
|
||
Neurokinin Receptor(393-407), rat (SPR393–407) 是一段属于大鼠神经激肽1受体(NK1R)的特定肽。它与P物质(SP)结合后,通过内吞作用迅速被NK1R内化,并循环至质膜。此化合物主要应用于神经源性炎症研究领域。 | |||
T76635 |
(Trp7,β-Ala8)-Neurokinin A (4-10)
|
||
(Trp7,β-Ala8)-Neurokinin A (4-10) 是一种有效的neurokinin-3 (NK3)拮抗剂。 | |||
T75742 |
Neurokinin A(4-10) TFA
|
||
Neurokinin A (4-10) TFA 是速激肽NK2受体激动剂。 | |||
T76435 |
Biotin-NeurokininA
|
||
Biotin-NeurokininA 是一种生物素化的NeurokininA. Neurokinin A (Substance K) 是速激肽家族的一种肽类神经递质,通过 NK-2 受体发挥作用。在人气道和胃肠道组织中作为主要的介体。 | |||
TP2455 |
Locustapyrokinin II
Pglu-ser-val-pro-thr-phe-thr-pro-arg-leu-NH2 |
||
Locustapyrokinin II is a member of the FXPRL-amide peptide family isolated from Locusta migratoria. | |||
TP1100 |
[bAla8]-Neurokinin A(4-10)
MEN 10210 |
||
[bAla8]-Neurokinin A(4-10) is a neurokinin 2 (NK2) receptor agonist. | |||
T82511 |
Ebdarokimab
|
||
Ebdarokimab (AK101),一种人源化IgG1-κ抗体,其表达系统主要选用CHO(中国仓鼠卵巢)细胞。 | |||
TP1363 |
Neurokinin B
|
||
Neurokinin B (NKB) belongs in the family of tachykinin peptides. Neurokinin B is implicated in a variety of human functions and pathways such as the secretion of gonadotropin-releasing hormone. | |||
T22516 |
5,7-Dichlorokynurenic acid sodium salt
|
Others | Others |
5,7-Dichlorokynurenic acid sodium salt is a NMDA receptor antagonist. | |||
T71760 |
4-Chlorokynurenine
|
Others | Others |
4-Chlorokynurenine is a prodrug of 7-Cl-kynurenic acid (7-Cl-KYNA), a potent, selective antagonist of the NMDA/glycine receptor. | |||
T124721 |
7,8-Dihydrokawain-5-ol
|
Others | Others |
7,8-Dihydrokawain-5-ol 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 T124721,CAS号为 52247-81-1。 | |||
T76426 |
[Lys5,MeLeu9,Nle10]Neurokinin A(4-10)
|
||
[Lys5,MeLeu9,Nle10]Neurokinin A(4-10) (LMN-NKA),Neurokinin A 的类似物,是一种选择性且有效的 NK2R 激动剂。[Lys5,MeLeu9,Nle10]Neurokinin A(4-10) 具有促运动活性。[Lys5,MeLeu9,Nle10]Neurokinin A(4-10) 可用于研究 NK-2 受体在多种组织平滑肌收缩中的作用。 | |||
TP2472 |
Leucopyrokinin
Pglu-thr-ser-phe-thr-pro-arg-leu-NH2 |
||
Leucopyrokinin is a myotropic neuropeptide. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TQ0183 |
Narciclasine
水仙环素,Lycoricidinol |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Narciclasine (Lycoricidinol) 是一种植物生长调节剂。它通过调节Rho/Rho 激酶/LIM 激酶/cofilin 信号传导途径,大大增加GTP 酶RhoA 活性以及以RhoA 依赖性方式诱导肌动蛋白应力纤维形成。 | |||
TN2029 |
p-Hydroxy-5,6-dehydrokawain
4'-Hydroxydehydrokawain,4'-羟基-5,6-脱氢醉椒素 |
Others | Others |
p-Hydroxy-5,6-dehydrokawain (4'-Hydroxydehydrokawain) 是一种分离自 Kawain 的天然产物。 | |||
TN1204 |
2,3-Dehydrokievitone
2,3-脱氢维酮 |
Antifungal | Microbiology/Virology |
2,3-Dehydrokievitone 是一种从刺桐属植物 Erythrina sacleuxii 中提取的一种异黄酮,具有抗菌活性,可通过降低α-溶血素表达来对抗耐甲氧西林金黄色葡萄球菌感染。 | |||
TN1406 |
Dihydrokaempferol
香橙素,Aromadendrin |
Apoptosis; BCL | Apoptosis |
Dihydrokaempferol (Aromadendrin) 是从紫荆花中分离得到的一种天然产物,诱导凋亡并抑制 Bcl-2 和 Bcl-xL 的表达,可以作为抗关节炎的良好新药候选。 | |||
T10191L |
7-Chlorokynurenic acid
7-chloro-4-hydroxy-2-carboxyquinoline,7-氯犬尿酸,7-CKA |
GluR; NMDAR | Neuroscience |
7-Chlorokynurenic acid (7-chloro-4-hydroxy-2-carboxyquinoline) 是一种有效的选择性 NMDA 受体拮抗剂,对甘氨酸 B 激动剂位点的 IC50 为 0.56 μM。 7-Chlorokynurenic acid 抑制谷氨酸再摄取到突触小泡中,Ki 为 0.59 μM,并在神经轴输送后显示出镇痛作用。 | |||
T4591 |
Dihydrokavain
Marindinin,二氢醉椒素,7,8-Dihydrokavain,7,8-Dihydrokawain |
Others | Others |
Dihydrokavain (Marindinin) 是一种具有抗焦虑作用的天然化合物。 | |||
TN5039 |
Sorokinianin
|
Antifection | Microbiology/Virology |
Sorokinianin is a phytotoxin, it has antifungal activity, it is highly effective in suppressing spore germination of F. solani (75%) at 100 ug/ml concentration. | |||
TN2987 |
3Alaph-Tigloyloxypterokaurene L3
|
Others | Others |
3Alaph-Tigloyloxypterokaurene L3 is a natural product from Wedelia trilobata. | |||
TN2921 |
3alpha-Cinnamoyloxypterokaurene L3
|
Others | Others |
3alpha-Cinnamoyloxypterokaurene L3 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2921,CAS号为 79406-13-6。 | |||
TN2920 |
3alpha-Angeloyloxypterokaurene L3
|
Others | Others |
3alpha-Angeloyloxypterokaurene L3 is a natural product from Wedelia trilobata. | |||
TN4854 |
Pterokaurene L3
|
Others | Others |
Pterokaurene L3 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4854,CAS号为 77658-38-9。 | |||
TN4853 |
Pterokaurane R
|
Others | Others |
Pterokaurane R 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4853,CAS号为 67349-43-3。 | |||
TN6178 |
Dihydrokaempferol 3-O-glucoside
香橙素-3-O-葡萄糖苷,Aromadendrin 3-O-glucoside |
||
Dihydrokaempferol 3-O-glucoside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6178,CAS号为 31049-08-8。 | |||
TN6375 |
Dihydrokaempferide
二氢山奈素,Aromadendrin 4'-methyl ether |
||
Dihydrokaempferide 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6375,CAS号为 137225-59-3。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-00904 |
Urokinase/uPA Protein, Human, Recombinant (His)
u-PA,QPD,BDPLT5,ATF,UPA,plasminogen activator, urok... |
Human | HEK293 Cells |
Urokinase/uPA Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 46 kDa and the accession number is A0A024QZM9. | |||
TMPY-00519 |
Gastrokine 1 Protein, Human, Recombinant (His)
UNQ489/PRO1005,CA11,foveolin,BRICD1,AMP18,gastrokin... |
Human | Baculovirus Insect Cells |
Gastrokine 1 (GKN1) belongs to the BRICHOS domain family and plays a major role in maintaining gastric mucosa integrity. GKN1 is highly expressed in gastric tissue and is secreted into the stomach but is not expressed in gastric cancer. GKN1-mediated inhibition of APP processing might represent a new approach for the prevention and therapy of Alzheimer's disease (AD). In the presence of GKN2, GKN1 loses its ability to decrease cell proliferation, induce apoptosis, and inhibit epigenetic alterati... | |||
TMPK-00972 |
PK-1/PROK1 Protein, Mouse, Recombinant (hFc)
PROK1,Mambakine,Prokineticin-1,EG-VEGF |
Mouse | HEK293 Cells |
PK-1 (Ac10) is a baculovirus-encoded serine/threonine kinase,a pk-1 knockout AcMNPV failed to produce infectious progeny, while the pk-1 repair virus could rescue this defect.the kinase activity of PK-1 is essential in regulating viral propagation. Electron microscopy revealed that pk-1 deletion affected the formation of normal nucleocapsids.PK-1 appears to phosphorylate some viral or cellular proteins that are essential for DNA packaging to regulate nucleocapsid assembly. | |||
TMPY-00274 |
Enterokinase Protein, Bovine, Recombinant (His)
transmembrane protease, serine 15 |
Bovine | P. pastoris (Yeast) |
Enterokinase Protein, Bovine, Recombinant (His) is expressed in yeast with His tag. The predicted molecular weight is 27.1 kDa and the accession number is P98072-1. | |||
TMPY-04626 |
Enterokinase/EK Protein, Bovine, Recombinant
EK, Enterokinase, PRSS7, Enteropeptidase, EC 3.4.21... |
Bovine | P. pastoris (Yeast) |
Enterokinase is a member of the trypsin family of serine proteases. The precursor protein is cleaved into two chains which then forms a heterodimer linked by a disulfide bond. The heavy chain anchors enterokinase in the intestinal brush border membrane and the light chain is the catalytic subunit, which initiates conversion activation of a subset of pancreatic proteolytic proenzymes. Enterokinase is the physiological activator of trypsinogen and has a specificity for the sequence (Asp)4-Lys-Ile.... | |||
TMPY-04504 |
Urokinase/uPA Protein, Rat, Recombinant (His)
plasminogen activator, urokinase |
Rat | HEK293 Cells |
Urokinase/uPA Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 47.3 kDa and the accession number is A6KKR2. | |||
TMPY-02945 |
Prokineticin 1/EG-VEGF Protein, Human, Recombinant (His)
PK1,EGVEGF,PRK1,prokineticin 1 |
Human | Baculovirus Insect Cells |
EG-VEGF, also known as prokineticin-1, is a member of the AVIT (prokineticin) family. Prokineticins are secreted proteins that can promote angiogenesis and induce strong gastrointestinal smooth muscle contraction. EG-VEGF can be detected in the steroidogenic glands, ovary, testis, adrenal and placenta. EG-VEGF has little or no effect on a variety of other endothelial and non-endothelial cell types. It induces proliferation, migration and fenestration (the formation of membrane discontinuities) i... | |||
TMPY-04559 |
CDC42BPB Protein, Human, Recombinant (His & GST)
CDC42 binding protein kinase beta (DMPK-like),MRCKB,CDC42 bi... |
Human | Baculovirus Insect Cells |
CDC42BPB is a member of the serine / threonine protein kinase family that contains a Cdc42 / Rsc-binding p21 binding domain similar to that of PAK kinase. The kinase domain of this protein is related to the myotonic dystrophy kinase related ROK and this kinase may have functions in downstream regulating of Cdc42 in cytoskeletal recognization. It has been reported that the CDC42BPB protein take part in regulating numerous cellular functions by binding to members of a serine / threonine protein ki... |