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Mouse Anti-IGF2BP1 Recombinant Antibody (CBYY-I1205) (CBMAB-I2374-YY)

This product is Mouse antibody that recognizes IGF2BP1. The antibody CBYY-I1205 can be used for immunoassay techniques such as: IP, RIA, WB
See all IGF2BP1 antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBYY-I1205
Antibody Isotype
IgG2a, κ
Application
IP, RIA, WB

Basic Information

Specificity
Human
Antibody Isotype
IgG2a, κ
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
50% glycerol, pH 7.2
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
IGF2BP1
Introduction
This gene encodes a member of the insulin-like growth factor 2 mRNA-binding protein family. The protein encoded by this gene contains four K homology domains and two RNA recognition motifs. It functions by binding to the mRNAs of certain genes, including insulin-like growth factor 2, beta-actin and beta-transducin repeat-containing protein, and regulating their translation. Two transcript variants encoding different isoforms have been found for this gene.
Entrez Gene ID
UniProt ID
Alternative Names
Insulin Like Growth Factor 2 MRNA Binding Protein 1
Function
RNA-binding factor that recruits target transcripts to cytoplasmic protein-RNA complexes (mRNPs). This transcript 'caging' into mRNPs allows mRNA transport and transient storage. It also modulates the rate and location at which target transcripts encounter the translational apparatus and shields them from endonuclease attacks or microRNA-mediated degradation. Plays a direct role in the transport and translation of transcripts required for axonal regeneration in adult sensory neurons (By similarity).

Regulates localized beta-actin/ACTB mRNA translation, a crucial process for cell polarity, cell migration and neurite outgrowth. Co-transcriptionally associates with the ACTB mRNA in the nucleus. This binding involves a conserved 54-nucleotide element in the ACTB mRNA 3'-UTR, known as the 'zipcode'. The RNP thus formed is exported to the cytoplasm, binds to a motor protein and is transported along the cytoskeleton to the cell periphery. During transport, prevents ACTB mRNA from being translated into protein. When the RNP complex reaches its destination near the plasma membrane, IGF2BP1 is phosphorylated. This releases the mRNA, allowing ribosomal 40S and 60S subunits to assemble and initiate ACTB protein synthesis. Monomeric ACTB then assembles into the subcortical actin cytoskeleton (By similarity).

During neuronal development, key regulator of neurite outgrowth, growth cone guidance and neuronal cell migration, presumably through the spatiotemporal fine tuning of protein synthesis, such as that of ACTB (By similarity).

May regulate mRNA transport to activated synapses (By similarity).

Binds to and stabilizes ABCB1/MDR-1 mRNA (By similarity).

During interstinal wound repair, interacts with and stabilizes PTGS2 transcript. PTGS2 mRNA stabilization may be crucial for colonic mucosal wound healing (By similarity).

Binds to the 3'-UTR of IGF2 mRNA by a mechanism of cooperative and sequential dimerization and regulates IGF2 mRNA subcellular localization and translation. Binds to MYC mRNA, in the coding region instability determinant (CRD) of the open reading frame (ORF), hence prevents MYC cleavage by endonucleases and possibly microRNA targeting to MYC-CRD. Binds to the 3'-UTR of CD44 mRNA and stabilizes it, hence promotes cell adhesion and invadopodia formation in cancer cells. Binds to the oncofetal H19 transcript and to the neuron-specific TAU mRNA and regulates their localizations. Binds to and stabilizes BTRC/FBW1A mRNA. Binds to the adenine-rich autoregulatory sequence (ARS) located in PABPC1 mRNA and represses its translation. PABPC1 mRNA-binding is stimulated by PABPC1 protein. Prevents BTRC/FBW1A mRNA degradation by disrupting microRNA-dependent interaction with AGO2. Promotes the directed movement of tumor-derived cells by fine-tuning intracellular signaling networks. Binds to MAPK4 3'-UTR and inhibits its translation. Interacts with PTEN transcript open reading frame (ORF) and prevents mRNA decay. This combined action on MAPK4 (down-regulation) and PTEN (up-regulation) antagonizes HSPB1 phosphorylation, consequently it prevents G-actin sequestration by phosphorylated HSPB1, allowing F-actin polymerization. Hence enhances the velocity of cell migration and stimulates directed cell migration by PTEN-modulated polarization. Interacts with Hepatitis C virus (HCV) 5'-UTR and 3'-UTR and specifically enhances translation at the HCV IRES, but not 5'-cap-dependent translation, possibly by recruiting eIF3. Interacts with HIV-1 GAG protein and blocks the formation of infectious HIV-1 particles. Reduces HIV-1 assembly by inhibiting viral RNA packaging, as well as assembly and processing of GAG protein on cellular membranes. During cellular stress, such as oxidative stress or heat shock, stabilizes target mRNAs that are recruited to stress granules, including CD44, IGF2, MAPK4, MYC, PTEN, RAPGEF2 and RPS6KA5 transcripts.
Biological Process
CRD-mediated mRNA stabilization Source: UniProtKB
Dendrite arborization Source: Ensembl
mRNA transport Source: UniProtKB-KW
Negative regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay Source: ComplexPortal
Negative regulation of translation Source: BHF-UCL
Nervous system development Source: GO_Central
Neuronal stem cell population maintenance Source: Ensembl
Pallium cell proliferation in forebrain Source: Ensembl
Positive regulation of cytoplasmic translation Source: ComplexPortal
Regulation of cytokine production Source: BHF-UCL
Regulation of gene expression Source: GO_Central
Regulation of mRNA stability involved in response to stress Source: UniProtKB
Regulation of RNA metabolic process Source: GO_Central
Cellular Location
Nucleus; Cytoplasm; Perinuclear region; Lamellipodium; Dendrite; Dendritic spine; Growth cone; Filopodium; Axon. In the nucleus, located in discrete foci, coinciding with the sites of ACTB transcription (By similarity). In the cytoplasm, localizes in cytoplasmic mRNP granules. Colocalizes with microtubules in growth cone filopodia and along neurites in neuronal cells (By similarity). Cytoplasmic colocalization with ACTB mRNA is partially lost at the cell periphery, suggesting release of the transcript. In neuronal processes, exhibits fast retrograde and anterograde movements, when associated with ACTB mRNA; this motility is lost when the association is inhibited (By similarity). In hippocampal neurons, predominantly located within dendrites, particularly at dendritic branching points in young cells, compared to axons (By similarity). In axons, predominantly found in axonal branches and their growth cones (By similarity). In motile cells, such as migrating fibroblasts, localizes to leading edges where it colocalizes with microtubules and microfilaments and to retracting tails (By similarity). Dendritic levels are regulated by neuronal activity and glutaminergic signals: they are increased by KCl-induced depolarization, which induces rapid efflux from the cell body into dendrites, and decreased by the NMDA receptor agonist (By similarity). In motile cells, transported towards the leading edge into the cortical region of the lamellipodia where it is connected to microfilaments (By similarity). In response to cellular stress, such as oxidative stress or heat shock, recruited to stress granules, but not to processing bodies.
PTM
Phosphorylated. Phosphorylation may impair association with ACTB mRNA and hence abolishes translational repression (By similarity).

Liu, Y., Guo, Q., Yang, H., Zhang, X. W., Feng, N., Wang, J. K., ... & Tu, P. F. (2022). Allosteric regulation of IGF2BP1 as a novel strategy for the activation of tumor immune microenvironment. ACS central science, 8(8), 1102-1115.

Núñez, L., Buxbaum, A. R., Katz, Z. B., Lopez-Jones, M., Nwokafor, C., Czaplinski, K., ... & Singer, R. H. (2022). Tagged actin mRNA dysregulation in IGF2BP1−/− mice. Proceedings of the National Academy of Sciences, 119(37), e2208465119.

Wallis, N., Oberman, F., Shurrush, K., Germain, N., Greenwald, G., Gershon, T., ... & Yisraeli, J. K. (2022). Small molecule inhibitor of Igf2bp1 represses Kras and a pro-oncogenic phenotype in cancer cells. RNA biology, 19(1), 26-43.

Glaß, M., Misiak, D., Bley, N., Müller, S., Hagemann, S., Busch, B., ... & Hüttelmaier, S. (2021). IGF2BP1, a conserved regulator of RNA turnover in cancer. Frontiers in Molecular Biosciences, 8, 632219.

Haase, J., Misiak, D., Bauer, M., Pazaitis, N., Braun, J., Pötschke, R., ... & Hüttelmaier, S. (2021). IGF2BP1 is the first positive marker for anaplastic thyroid carcinoma diagnosis. Modern Pathology, 34(1), 32-41.

Wang, K., Hu, H., Tian, Y., Li, J., Scheben, A., Zhang, C., ... & Kang, X. (2021). The chicken pan-genome reveals gene content variation and a promoter region deletion in IGF2BP1 affecting body size. Molecular Biology and Evolution, 38(11), 5066-5081.

Huang, Q., Guo, H., Wang, S., Ma, Y., Chen, H., Li, H., ... & Wang, J. (2020). A novel circular RNA, circXPO1, promotes lung adenocarcinoma progression by interacting with IGF2BP1. Cell death & disease, 11(12), 1031.

Zhu, S., Wang, J. Z., Chen, D., He, Y. T., Meng, N., Chen, M., ... & Yan, G. R. (2020). An oncopeptide regulates m6A recognition by the m6A reader IGF2BP1 and tumorigenesis. Nature communications, 11(1), 1685.

Müller, S., Glaß, M., Singh, A. K., Haase, J., Bley, N., Fuchs, T., ... & Hüttelmaier, S. (2019). IGF2BP1 promotes SRF-dependent transcription in cancer in a m6A-and miRNA-dependent manner. Nucleic acids research, 47(1), 375-390.

Müller, S., Bley, N., Glaß, M., Busch, B., Rousseau, V., Misiak, D., ... & Hüttelmaier, S. (2018). IGF2BP1 enhances an aggressive tumor cell phenotype by impairing miRNA-directed downregulation of oncogenic factors. Nucleic acids research, 46(12), 6285-6303.

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

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