1132 Results for "

recombinant

" in MedChemExpress (MCE) Product Catalog:
Products (1132)

1132 Results for "recombinant" in MCE Product Catalog:

224
224 Publications Verification
Art. -Nr.: HY-18085
CAS. Nr.: 117-39-5
Quercetin, a natural flavonoid, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4 μM, 3.0 μM and 5.4 μM for PI3K γ, PI3K δ and PI3K β, respectively .
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223
223 Cited Publications
Art. -Nr.: HY-18085A
CAS. Nr.: 849061-97-8
Quercetin hydrate, a natural flavonoid, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4 μM, 3.0 μM and 5.4 μM for PI3K γ, PI3K δ and PI3K β, respectively .
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218
218 Cited Publications
Art. -Nr.: HY-N0146
CAS. Nr.: 6151-25-3
Quercetin dihydrate, a natural flavonoid, is a stimulator of recombinant SIRT1 and a PI3K inhibitor with IC50s of 2.4 μM, 3.0 μM and 5.4 μM for PI3K γ, PI3K δ and PI3K β, respectively .
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141
141 Cited Publications
Art. -Nr.: HY-10295A
CAS. Nr.: 350228-36-3
Reinheit:  99.66%
Forschungsgebiete:  

Neurological Disease Cancer

SB 202190 hydrochloride is a selective p38 MAP kinase inhibitor with IC50s of 50 nM and 100 nM for p38α and p38β2, respectively. SB 202190 hydrochloride binds to the ATP pocket of the active recombinant human p38 kinase with a Kd of 38 nM. SB 202190 hydrochloride has anti-cancer activity . SB202190 hydrochloride induces autophagy .
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141
141 Cited Publications
Art. -Nr.: HY-10295
CAS. Nr.: 152121-30-7
Reinheit:  99.89%
Forschungsgebiete:  

Neurological Disease Cancer

SB 202190 is a selective p38 MAP kinase inhibitor with IC50s of 50 nM and 100 nM for p38α and p38β2, respectively. SB 202190 binds to the ATP pocket of the active recombinant human p38 kinase with a Kd of 38 nM. SB 202190 has anti-cancer activity and rescued memory deficits . SB202190 induces autophagy .
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65
65 Cited Publications
Art. -Nr.: HY-K2014

MCE PEI Transfection Reagent is designed based on 25 kDa PEI. It has high-efficiency, low-toxicity, strong-stability, and is suitable for many cell types, such as HEK-293、HEK-293T、CHO-K1、COS-1、COS-7、NIH/3T3、Sf9、HepG2 and HeLa et, even some hard-to-transfect cells. It can also be applied to large-scale recombinant protein expression and virus production. The 1 mL is defined as the base specification. All larger sizes correspond to incremental volumes of this base.

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56
56 Cited Publications
Art. -Nr.: HY-108841
CAS. Nr.: 143090-92-0
Reinheit:  99.40%
Synonyms: Kineret; Anakinra

Target:  

Interleukin Related

Forschungsgebiete:  

Infection Inflammation/Immunology Cancer

Raleukin (Kineret) is a recombinant, nonglycosylated human interleukin-1 receptor (IL-1R) antagonist. Raleukin significantly reduces neutrophil accumulation in blood vessels and brain infarct volume as well as improves motor coordination performance in ischemic stroke mice model. Anakinra can be used to study chronic inflammatory disorders like rheumatoid arthritis and cardiovascular recurrence post-myocardial infarction .
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40
40 Cited Publications
Art. -Nr.: HY-108882A
CAS. Nr.: 9003-98-9
Target:  

Endonuclease

Forschungsgebiete:  

Others

Recombinant DNase I (RNase-free) is a recombinant deoxyribonuclease that degrades DNA. Recombinant DNase I is essential for limiting inflammatory responses and maintaining homeostasis .
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39
39 Cited Publications
Art. -Nr.: HY-10461
CAS. Nr.: 869288-64-2
Reinheit:  99.25%
Target:  

FAK Apoptosis

Forschungsgebiete:  

Cancer

PF-573228 is a potent and selective FAK inhibitor with IC50 of 4 nM for purified recombinant catalytic fragment of FAK.
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37
37 Cited Publications
Art. -Nr.: HY-19805
CAS. Nr.: 52029-86-4
Target:  

CaMK AMPK Autophagy

Forschungsgebiete:  

Metabolic Disease

STO-609 is a selective and cell-permeable inhibitor of the Ca 2+/calmodulin-dependent protein kinase kinase (CaM-KK), with Ki values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively. STO-609 inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC50 ~0.02 g/ml.
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33
33 Cited Publications
Art. -Nr.: HY-15418
CAS. Nr.: 300816-15-3
Reinheit:  99.23%
Target:  

CCR

Forschungsgebiete:  

Inflammation/Immunology Endocrinology

RS 504393 is a selective CCR2 chemokine receptor antagonist (IC50 values are 89 nM and > 100 μM for inhibition of human recombinant CCR2 and CCR1 receptors respectively).
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31
31 Cited Publications
Art. -Nr.: HY-111941
CAS. Nr.: 2361659-62-1
Reinheit:  99.62%
Target:  

IKK

GSK8612 is a highly selective and potent Tank-binding Kinase-1 (TBK1) inhibitor, with a pIC50 of 6.8 for recombinant TBK1 .
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31
31 Cited Publications
Art. -Nr.: HY-11068
CAS. Nr.: 193551-21-2
Reinheit:  99.15%
SB 239063 is a potent, selective and orally active p38 MAPK inhibitor, exhibits an IC50 of 44 nM for recombinant purified human p38α, with equipotent inhibitory activity against p38α and p38β. SB 239063 has no effect on p38γ or p38δ. With anti-asthma activity and also be used to enhance memory which is impaired due to aging or medical conditions, such as, AD. SB 239063 can penetrate the blood brain barrier (BBB) .
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26
26 Cited Publications
Art. -Nr.: HY-P0223
CAS. Nr.: 98849-88-8
Forschungsgebiete:  

Inflammation/Immunology

FLAG peptide is a multifunctional fusion tag for the purification of recombinant proteins. FLAG peptide maintances the natural folding of its fusing proteins. FLAG peptide can be removed by enterokinase, and eluted under non-denaturing conditions .
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26
26 Cited Publications
Art. -Nr.: HY-P0223A
Forschungsgebiete:  

Others

FLAG peptide TFA is the TFA salt form of FLAG peptide (HY-P0223). FLAG peptide TFA is a multifunctional fusion tag for the purification of recombinant proteins. FLAG peptide TFA maintances the natural folding of its fusing proteins. FLAG peptide TFA can be removed by enterokinase, and eluted under non-denaturing conditions .
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21
21 Cited Publications
Art. -Nr.: HY-100463
CAS. Nr.: 79756-69-7
Reinheit:  ≥98.0%
Target:  

SHP1 Phosphatase

Forschungsgebiete:  

Inflammation/Immunology Cancer

TPI-1, also known as Tyrosine Phosphatase Inhibitor 1, is a SHP-1 inhibitor; inhibits recombinant SHP-1 with an IC50 of 40 nM.
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21
21 Cited Publications
Art. -Nr.: HY-K1033

RNase Inhibitor is a 50 kDa recombinant protein expressed in E.coli, and can specifically inhibit RNase A, B and C. The 10 KU volume is defined as the base specification. All larger sizes correspond to incremental volumes of this base.

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19
19 Cited Publications
Art. -Nr.: HY-108903
CAS. Nr.: 37326-33-3
Synonyms: Vorhyaluronidase alfa; rHuPH 20
Forschungsgebiete:  

Metabolic Disease

Hyaluronidase (human recombinant) (Vorhyaluronidase alfa; rHuPH 20) is an enzyme that catalyzes the degradation of hyaluronic acid. Hyaluronidase (human recombinant) is used to improve the absorption and dispersal of parenteral fluids, medications, and contrast media .
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18
18 Cited Publications
Art. -Nr.: HY-13863
CAS. Nr.: 1256493-34-1
Reinheit:  99.11%
Synonyms: Dyngo-4a
Target:  

Dynamin

Forschungsgebiete:  

Neurological Disease

Hydroxy Dynasore (Dyngo-4a), a structural mimetic analog of Dynasore (HY-15304), is an improved, less cytotoxic and versatile dynamin inhibitor with IC50 values ​​of 0.38 μM and 2.3 μM for brain recombinant dynamin I and recombinant mouse dynamin II, respectively. Hydroxy Dynasore inhibits dynamin-dependent transferrin endocytosis with an IC50 of 5.7 μM.
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17
17 Cited Publications
Art. -Nr.: HY-12795
CAS. Nr.: 1383716-33-3
Reinheit:  99.79%
Target:  

PI3K Autophagy

Forschungsgebiete:  

Cancer

Vps34-IN-1 is a potent and selective inhibitor of class III Vps34 PI3K. Vps34-IN-1 inhibits phosphorylation of PtdIns by recombinant insect cell expressed Vps34-Vps15 complex with an IC50 of ~25 nM. Vps34-IN-1 can suppress SGK3 activation by reducing PtdIns(3)P levels via lowering phosphorylation of T-loop and hydrophobic motifs. Vps34-IN-1 modulates autophagy .
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