154 results for "ROCK1" in 产品

ROCK1 Products

Rho-associated kinase I (ROCK1, ROK beta, p160ROCK) is a serine-threonine protein kinase and an effector of the small GTPase Rho. With N-terminus protein kinase domain and C-terminus Rho-binding domain/pleckstrin homology domain, ROCK1 can be activated by either RhoA or RhoB. In Rho specific ROCK1 activation, a Rho protein binds to the Rho-binding domain and induces a conformational change which opens the kinase domain for the phosphorylation of downstream effectors (1). Activated ROCK1 ...

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Selective ROCK inhibitor; inhibits ROCK1 (p160 ROCK) and ROCK2; stem cell freezing (cryopreservation) media component

GMP Version Available: TB1254-GMP
GMP
Alternate Names: y27632,Y-27632 2HCl,ROCK inhibitor,ROCK1 inhibitor
Chemical Name: trans-4-[(1R)-1-Aminoethyl]-N-4-pyridinylcyclohexanecarboxamide dihydrochloride
Purity: ≥98%
ROCK inhibition by Y-27632 and immunostaining of skeletal myogenic differentiation of MESP1+ mesoderm,
(8)
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Y-27632 synthesized to cGMP guidelines

Chemical Name: trans-4-[(1R)-1-Aminoethyl]-N-4-pyridinylcyclohexanecarboxamide dihydrochloride
Purity: ≥99%
Y-27632 synthesized to cGMP guidelines
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ROCK inhibitor; improves the efficiency of fibroblast reprogramming and induction of iPSCs

Chemical Name: N-Benzyl-[2-(pyrimidin-4-yl)amino]thiazole-4-carboxamide
Purity: ≥98%
ROCK inhibitor ; improves the efficiency of fibroblast reprogramming and induction of iPSCs
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Selective Rho-kinase (ROCK) inhibitor

Chemical Name: (S)-(+)-2-Methyl-1-[(4-methyl-5-isoquinolinyl)sulfonyl]-hexahydro-1H-1,4-diazepine dihydrochloride
Purity: ≥98%
Selective Rho-kinase (ROCK) inhibitor
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Reactivity: Human, Mouse, Rat
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, Mycoplasma
Western Blot: ROCK1 Antibody [NBP1-82450]
(4)
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Inhibitor of cyclic nucleotide dependent- and Rho-kinases

Alternate Names: HA 1077
Purity: ≥98%
Inhibitor of cyclic nucleotide dependent- and Rho-kinases
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Reactivity: Human, Mouse, Rat
Details: Mouse IgG1 Monoclonal Clone #261
Applications: WB
Western Blot: ROCK1 Antibody (261) [NBP2-42917]
(6)
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Reactivity: Human, Mouse, Rat
Details: Mouse IgG2B Monoclonal Clone #464
Applications: WB
Western Blot: ROCK1 Antibody (464) [NBP2-42918]
(6)
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Reactivity: Human, Mouse
Details: Rabbit IgG Polyclonal
Applications: KO, IHC, WB
ROCK1 Antibody - BSA Free
(4)
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Reactivity: Human
Details: Mouse IgG1 kappa Monoclonal Clone #2E2
Applications: WB, ELISA, ICC/IF
Western Blot: ROCK1 Antibody (2E2) [H00006093-M01]
(3)
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Potent and selective ROCK inhibitor

Chemical Name: N-[3-[[2-(4-Amino-1,2,5-oxadiazol-3-yl)-1-ethyl-1H-imidazo[4,5-c]pyridin-6-yl]oxy]phenyl]-4-[2-(4-morpholinyl)ethoxy]benzamide
Purity: ≥98%
Potent and selective ROCK inhibitor
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Reactivity: Human
Source: Sf 9 (baculovirus)
Accession #: NM_005406
Applications: Bioactivity
Recombinant Human Active ROCK1 Protein SDS-PAGE
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Selective Rho-kinase (ROCK) inhibitor. More selective analog of H 1152 dihydrochloride (Cat. No. 2414)

Chemical Name: (S)-(+)-4-Glycyl-2-methyl-1-[(4-methyl-5-isoquinolinyl)sulfonyl]-hexahydro-1H-1,4-diazepine dihydrochloride
Purity: ≥98%
Selective Rho-kinase (ROCK) inhibitor. More selective analog of H 1152 dihydrochloride (Cat. No. 2414)
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Potent Rho-kinase inhibitor; vasodilator

Chemical Name: (3S)-1-[[2-(4-Amino-1,2,5-oxadiazol-3-yl)-1-ethyl-1H-imidazo[4,5-c]pyridin-7-yl]carbonyl]-3-pyrrolidinamine dihydrochloride
Purity: ≥98%
Potent Rho-kinase inhibitor; vasodilator
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Potent and highly selective ROCK inhibitor; orally active

Alternate Names: Azaindole-1,BAY-549
Chemical Name: 6-Chloro-N4-[3,5-difluoro-4-[(3-methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]phenyl]-2,4-pyrimidinediamine
Purity: ≥98%
Potent and highly selective ROCK inhibitor; orally active
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Potent and selective ROCK inhibitor; antitumor

Chemical Name: N-[(3-Hydroxyphenyl)methyl]-N'-[4-(4-pyridinyl)-2-thiazolyl]urea dihydrochloride
Purity: ≥98%
Potent and selective ROCK inhibitor; antitumor
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Potent ROCK inhibitor

Chemical Name: 2-Fluoro-N-[[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)phenyl]methyl]benzenemethanamine dihydrochloride
Purity: ≥98%
Potent ROCK inhibitor
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Potent and selective LIMK inhibitor; antitumor

Chemical Name: N-(2-Hydroxyethyl)-N'-[4,5-methyl-7H-pyrrolo[2,3-d]pyrimidine-4-yl)phenyl]-N-phenylurea
Purity: ≥98%
Potent and selective LIMK inhibitor; antitumor
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Sterile-filtered 10 mM solution of Y-27632, selective ROCK inhibitor, pre-dissolved in water

Chemical Name: trans-4-[(1R)-1-Aminoethyl]-N-4-pyridinylcyclohexanecarboxamide dihydrochloride
Purity: ≥97%
vial of Y-27632 in solution
(2)
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Potent and selective ROCK inhibitor; orally bioavailable and brain penetrant

Chemical Name: (2R)-4-(3-Fluoro-4-pyridinyl)-N-[(1R)-1-(3-methoxyphenyl)ethyl]-2-methyl-1-piperazinecarboxamide
Purity: ≥98%
Potent and selective ROCK2 inhibitor; orally bioavailable and brain penetrant
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