R

RSK2 (PT0827R) PT™ Rabbit mAb

-YM8501

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Catalog: YM8501
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

40μL
$190.00
In stock

0

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Main Information
Target

RSK2

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, IHC, IF, IP, ELISA

MW

84kD (Calculated)

84kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
IHC 1:1000-1:5000; WB 1:2000-1:10000; IF 1:200-1:1000; ELISA 1:5000-1:20000; IP 1:50-1:200;
Formulation
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Specificity
Endogenous
Purification
Protein A
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
MW(Calculated)
84kD
MW(Observed)
84kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
PT0827R
Isotype
IgG,Kappa
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RS0002

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Antigen&Target Information
Specificity:
Endogenous
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Gene Name:
RPS6KA3 ISPK1 MAPKAPK1B RSK2
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Protein Name:
RSK2
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Other Name:
Ribosomal protein S6 kinase alpha-3 ;
S6K-alpha-3 ;
90 kDa ribosomal protein S6 kinase 3 ;
p90-RSK 3 ;
p90RSK3 ;
Insulin-stimulated protein kinase 1 ;
ISPK-1 ;
MAP kinase-activated protein kinase 1b ;
MAPK-activated protein kinase 1b ;
MAPKAP kinase 1b ;
MAPKAPK-1b ;
Ribosomal S6 kinase 2 ;
RSK-2 ;
pp90RSK2 ;
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Database Link:
Organism Gene ID SwissProt
Human 6777; P51812;
Mouse 110651; P18654;
Rat 25126; P52632;
Background:
ribosomal protein S6 kinase A3(RPS6KA3) Homo sapiens This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains 2 non-identical kinase catalytic domains and phosphorylates various substrates, including members of the mitogen-activated kinase (MAPK) signalling pathway. The activity of this protein has been implicated in controlling cell growth and differentiation. Mutations in this gene have been associated with Coffin-Lowry syndrome (CLS). [provided by RefSeq, Jul 2008],
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Function:
Catalytic activity:ATP + a protein = ADP + a phosphoprotein.,cofactor:Magnesium.,Disease:Defects in RPS6KA3 are the cause of Coffin-Lowry syndrome (CLS) [MIM:303600]; an X-linked dominant disorder characterized by severe mental retardation with facial and digital dysmorphisms, and progressive skeletal deformations.,enzyme regulation:Activated by multiple phosphorylations on threonine and serine residues.,Function:Serine/threonine kinase that may play a role in mediating the growth-factor and stress induced activation of the transcription factor CREB.,PTM:Autophosphorylated on Ser-386, as part of the activation process.,PTM:Ser-227 phosphorylation promotes Ser-386 phosphorylation and leads to basal activation. Full activation by growth factors requires additional phosphorylation on Ser-369.,similarity:Belongs to the protein kinase superfamily. AGC Ser/Thr protein kinase family. S6 kinase subfamily.,similarity:Contains 1 AGC-kinase C-terminal domain.,similarity:Contains 2 protein kinase domains.,subunit:Forms a complex with either ERK1 or ERK2 in quiescent cells. Transiently dissociates following mitogenic stimulation (By similarity). Interacts with NFATC4.,tissue specificity:Expressed in many tissues, highest levels in skeletal muscle.,
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Cellular Localization:
Nucleus . Cytoplasm .
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Tissue Expression:
Research Areas:
>>ErbB signaling pathway ;
>>Chemokine signaling pathway ;
>>Necroptosis ;
>>JAK-STAT signaling pathway ;
>>Th1 and Th2 cell differentiation ;
>>Th17 cell differentiation ;
>>Prolactin signaling pathway ;
>>AGE-RAGE signaling pathway in diabetic complications ;
>>Growth hormone synthesis, secretion and action ;
>>Hepatitis B ;
>>Measles ;
>>Human T-cell leukemia virus 1 infection ;
>>Pathways in cancer ;
>>Viral carcinogenesis ;
>>Chemical carcinogenesis - receptor activation ;
>>Chronic myeloid leukemia ;
>>Acute myeloid leukemia ;
>>Non-small cell lung cancer
show all
Catalog: YM8501
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

40μL
$190.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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