307 results for "JNK2" in Products

JNK2 Products

Members of the MAPK family, the c-Jun N-terminal kinases (JNKs) are activated by environmental stresses and inflammatory cytokines. Ten JNK isoforms are created by alternative splicing of mRNA transcripts derived from three genes: JNK1, JNK2, and JNK3. All JNKs are activated by dual phosphorylation; at T183/Y185 for JNK1 and 2, and T221/Y223 for JNK3. Activated JNKs translocate to the nucleus where they regulate the activity of several transcription factors; including the c-Jun component of AP-1 and ATF-2.

Reactivity: Human, Mouse, Rat
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, Simple Western
Detection of Human and Mouse Phospho-JNK (T183/Y185) antibody by Western Blot.
(12)
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Selective JNK inhibitor

Chemical Name: Anthra[1-9-cd]pyrazol-6(2H)-one
Purity: ≥98%
Selective JNK inhibitor
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Reactivity: Human, Mouse, Rat
Assay Range: 156-10000 pg/mL
Applications: ELISA
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Reactivity: Human, Mouse, Rat, Canine, Monkey
Details: Mouse IgG1 Monoclonal Clone #OTI1A1
Applications: IHC, WB, ICC/IF
Western Blot: JNK2 Antibody (OTI1A1) [NBP2-45815]
(7)
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Reactivity: Human, Mouse, Rat, Canine, Monkey
Details: Mouse IgG1 Monoclonal Clone #OTI1A1
Applications: IHC, WB, ICC/IF
Western Blot: JNK2 Antibody (OTI1A1)Azide and BSA Free [NBP2-71259]
(7)
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Inhibitor of JNK signaling

Chemical Name: (9S,10R,12R)-5-16-Bis[(ethylthio)methyl]-2,3,9,10,11,12-hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylic acid methyl ester
Purity: ≥97%
Inhibitor of JNK signaling
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Recombinant Monoclonal Antibody

Reactivity: Human
Details: Rabbit IgG Monoclonal Clone #011
Applications: IHC, WB, ELISA, ICC/IF, IP
Western Blot: JNK2 Antibody (011) [NBP2-89621]
(6)
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Reactivity: Human, Mouse, Rat, Insect
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, ICC/IF
Western Blot: JNK2 Antibody [NBP1-30905]
(5)
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Reactivity: Human, Mouse, Rat
Assay Range: 125-8000 pg/mL
Applications: ELISA
R&D Systems DuoSet ELISAs
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Selective JNK inhibitor

Chemical Name: N-(4-Amino-5-cyano-6-ethoxy-2-pyridinyl)-2,5-dimethoxybenzeneacetamide
Purity: ≥98%
Selective JNK inhibitor
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Selective JNK inhibitor

Alternate Names: Halicin
Chemical Name: 5-[(5-Nitro-2-thiazolyl)thio]-1,3,4thiadiazol-2-amine
Purity: ≥98%
Selective JNK inhibitor
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Selective inhibitor of JNK2 and JNK3

Chemical Name: N-(3-Cyano-4,5,6,7-tetrahydrobenzo[b]thienyl-2-yl)-1-naphthalenecarboxamide
Purity: ≥98%
Selective inhibitor of JNK2 and JNK3
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Selective, competitive JNK inhibitor

Chemical Name: 4-(2,3-Dihydro-1,4-benzodioxin-6-yl)-2,4-dihydro-5-[(5-nitro-2-thiazolyl)thio]-3H-1,2,4-triazol-3-one
Purity: ≥98%
Selective, competitive JNK inhibitor
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High affinity JNK inhibitor; also inhibits HCMV replication

Chemical Name: 3-[3-[2-(1-Piperidinyl)ethoxy]phenyl]-5-(1H-1,2,4-triazol-5-yl)-1H-indazole dihydrochloride
Purity: ≥98%
High affinity JNK inhibitor; also inhibits HCMV replication
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TCS JNK 6o synthesized to Ancillary Material Grade

Chemical Name: N-(4-Amino-5-cyano-6-ethoxy-2-pyridinyl)-2,5-dimethoxybenzeneacetamide
Purity: ≥98%
TCS JNK 6o synthesized to Ancillary Material Grade
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