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Mouse Anti-GPS2 Recombinant Antibody (16C53) (CBMAB-G0733-LY)

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Summary

Host Animal
Mouse
Specificity
Human
Clone
16C53
Antibody Isotype
IgG
Application
ELISA, WB

Basic Information

Immunogen
Recombinant protein corresponding to aa161-311 from human GPS2 expressed in E. coli
Specificity
Human
Antibody Isotype
IgG
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
10% glycerol
Preservative
0.02% NaN3
Concentration
1 mg/mL
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
G protein pathway suppressor 2
Introduction
This gene encodes a protein involved in G protein-mitogen-activated protein kinase (MAPK) signaling cascades. When overexpressed in mammalian cells, this gene could potently suppress a RAS- and MAPK-mediated signal and interfere with JNK activity, suggesting that the function of this gene may be signal repression. The encoded protein is an integral subunit of the NCOR1-HDAC3 (nuclear receptor corepressor 1-histone deacetylase 3) complex, and it was shown that the complex inhibits JNK activation through this subunit and thus could potentially provide an alternative mechanism for hormone-mediated antagonism of AP1 (activator protein 1) function. [provided by RefSeq, Jul 2008]
Entrez Gene ID
UniProt ID
Alternative Names
G Protein Pathway Suppressor 2; GPS-2; AMF-1;
Function
Key regulator of inflammation, lipid metabolism and mitochondrion homeostasis that acts by inhibiting the activity of the ubiquitin-conjugating enzyme UBE2N/Ubc13, thereby inhibiting 'Lys-63'-linked ubiquitination (By similarity).

In the nucleus, can both acts as a corepressor and coactivator of transcription, depending on the context (PubMed:24943844).

Acts as a transcription coactivator in adipocytes by promoting the recruitment of PPARG to promoters: acts by inhibiting the activity of the ubiquitin-conjugating enzyme UBE2N/Ubc13, leading to stabilization of KDM4A and subsequent histone H3 'Lys-9' (H3K9) demethylation (By similarity).

Promotes cholesterol efflux by acting as a transcription coactivator (PubMed:19481530).

Acts as a regulator of B-cell development by inhibiting UBE2N/Ubc13, thereby restricting the activation of Toll-like receptors (TLRs) and B-cell antigen receptors (BCRs) signaling pathways (By similarity).

Acts as a key mediator of mitochondrial stress response: in response to mitochondrial depolarization, relocates from the mitochondria to the nucleus following desumoylation and specifically promotes expression of nuclear-encoded mitochondrial genes (PubMed:29499132).

Promotes transcription of nuclear-encoded mitochondrial genes by inhibiting UBE2N/Ubc13 (PubMed:29499132).

Can also act as a corepressor as part of the N-Cor repressor complex by repressing active PPARG (PubMed:19858209, PubMed:24943844).

Plays an anti-inflammatory role in macrophages and is required for insulin sensitivity by acting as a corepressor (By similarity).

Plays an anti-inflammatory role during the hepatic acute phase response by interacting with sumoylated NR1H2 and NR5A2 proteins, thereby preventing N-Cor corepressor complex dissociation (PubMed:20159957).

In the cytosol, also plays a non-transcriptional role by regulating insulin signaling and pro-inflammatory pathways (By similarity).

In the cytoplasm, acts as a negative regulator of inflammation by inhibiting the proinflammatory TNF-alpha pathway; acts by repressing UBE2N/Ubc13 activity (By similarity).

In the cytoplasm of adipocytes, restricts the activation of insulin signaling via inhibition of UBE2N/Ubc13-mediated ubiquitination of AKT (By similarity).

Able to suppress G-protein- and mitogen-activated protein kinase-mediated signal transduction (PubMed:8943324).

Acts as a tumor-suppressor in liposarcoma (PubMed:27460081).

(Microbial infection) Required for efficient replication of hepatitis C virus (HCV) by promoting the interaction between VAPA and HCV virus protein NS5A.
Biological Process
B cell differentiation Source: UniProtKB
Inactivation of MAPK activity Source: ProtInc
JNK cascade Source: ProtInc
Negative regulation of B cell receptor signaling pathway Source: UniProtKB
Negative regulation of fat cell differentiation Source: UniProtKB
Negative regulation of inflammatory response Source: UniProtKB
Negative regulation of JNK cascade Source: UniProtKB
Negative regulation of protein K63-linked ubiquitination Source: UniProtKB
Negative regulation of toll-like receptor signaling pathway Source: UniProtKB
Negative regulation of transcription by RNA polymerase II Source: UniProtKB
Negative regulation of tumor necrosis factor-mediated signaling pathway Source: UniProtKB
Positive regulation of cholesterol efflux Source: UniProtKB
Positive regulation of peroxisome proliferator activated receptor signaling pathway Source: UniProtKB
Positive regulation of transcription by RNA polymerase II Source: UniProtKB
Regulation of fat cell differentiation Source: UniProtKB
Regulation of lipid metabolic process Source: UniProtKB
Response to mitochondrial depolarisation Source: UniProtKB
Cellular Location
Mitochondrion; Cytosol; Nucleus. Sumoylation regulates the subcellular location (PubMed:24943844). Relocates from the mitochondria to the nucleus following desumoylation, leading to mediate mitochondrial stress response (By similarity).
PTM
Sumoylation regulates its subcellular location (PubMed:24943844). Sumoylation at Lys-45 and Lys-71 regulates the shuttling between the cytoplasm and the nucleus (PubMed:24943844). Sumoylation at Lys-71 is required for interaction with TBL1X (By similarity). Sumoylated at Lys-45 and Lys-71 in mitochondrion (By similarity). Desumoylation by SENP1 leads to relocation from the mitochondria to the nucleus (By similarity).
Ubiquitinated at the C-terminus by SIAH2; leading to its degradation by the proteasome. Interaction with TBL1X and methylation at Arg-323 protect GPS2 against ubiquitination and degradation.
Methylated at Arg-312 and Arg-323 by PRMT6. Methylation at Arg-323 protects from degradation by the proteasome.
More Infomation

Shi, S., Chen, H., Wang, H., Wan, J., Shi, Y., Li, J., ... & Sun, F. (2022). Genome-wide CRISPR knockout screening identified G protein pathway suppressor 2 as a novel tumor suppressor for uveal melanoma metastasis. Journal of Cancer Research and Clinical Oncology, 1-12.

Huang, Z., Liang, N., Goñi, S., Damdimopoulos, A., Wang, C., Ballaire, R., ... & Treuter, E. (2021). The corepressors GPS2 and SMRT control enhancer and silencer remodeling via eRNA transcription during inflammatory activation of macrophages. Molecular cell, 81(5), 953-968.

Si, Y., Zhang, H., Peng, P., Zhu, C., Shen, J., Xiong, Y., ... & Liu, Y. (2021). G protein pathway suppressor 2 suppresses gastric cancer by destabilizing epidermal growth factor receptor. Cancer Science, 112(12), 4867-4882.

Gong, W., He, X., Huang, K., Zhang, Y., Li, C., Yang, Y., ... & Jin, M. (2021). Interaction of nuclear export protein with G protein pathway suppressor 2 (GPS2) facilitates influenza A virus replication by weakening the inhibition of GPS2 to RNA synthesis and ribonucleoprotein assembly. Journal of Virology, 95(10), e00008-21.

Chan, S., Smith, E., Gao, Y., Kwan, J., Blum, B. C., Tilston-Lunel, A. M., ... & Perissi, V. (2021). Loss of G-protein pathway suppressor 2 promotes tumor growth through activation of AKT signaling. Frontiers in Cell and Developmental Biology, 1667.

Ma, W. B., Wang, X. H., Li, C. Y., Tian, H. H., Zhang, J., Bi, J. J., ... & Yin, R. H. (2020). GPS2 promotes erythroid differentiation by control of the stability of EKLF protein. Blood, 135(25), 2302-2315.

Huang, Z., Liang, N., Damdimopoulos, A., Fan, R., & Treuter, E. (2019). G protein pathway suppressor 2 (GPS2) links inflammation and cholesterol efflux by controlling lipopolysaccharide‐induced ATP‐binding cassette transporter A1 expression in macrophages. The FASEB Journal, 33(2), 1631-1643.

Liang, N., Damdimopoulos, A., Goñi, S., Huang, Z., Vedin, L. L., Jakobsson, T., ... & Fan, R. (2019). Hepatocyte-specific loss of GPS2 in mice reduces non-alcoholic steatohepatitis via activation of PPARα. Nature communications, 10(1), 1684.

Cardamone, M. D., Tanasa, B., Cederquist, C. T., Huang, J., Mahdaviani, K., Li, W., ... & Perissi, V. (2018). Mitochondrial retrograde signaling in mammals is mediated by the transcriptional cofactor GPS2 via direct mitochondria-to-nucleus translocation. Molecular cell, 69(5), 757-772.

Zhuang, Z., Xiao, J., Chen, X., Hu, X., Li, R., Chen, S., ... & Cai, H. (2018). G protein pathway suppressor 2 enhanced the renal large-conductance Ca2+-activated potassium channel expression via inhibiting ERK1/2 signaling pathway. American Journal of Physiology-Renal Physiology, 315(3), F503-F511.

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For research use only. Not intended for any clinical use.

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