Recombinant Mouse HNRNPA2B1 Protein (1-353 aa), His-SUMO-tagged
Cat.No. : | HNRNPA2B1-2196M |
Product Overview : | Recombinant Mouse HNRNPA2B1 Protein (1-353 aa) is produced by E. coli expression system. This protein is fused with a 6xHis-SUMO tag at the N-terminal. Protein Description: Full Length. |
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Description : | Heterogeneous nuclear ribonucleoprotein (hnRNP) that associates with nascent pre-mRNAs, packaging them into hnRNP particles. The hnRNP particle arrangement on nascent hnRNA is non-random and sequence-dependent and serves to condense and stabilize the transcripts and minimize tangling and knotting. Packaging plays a role in various processes such as transcription, pre-mRNA processing, RNA nuclear export, subcellular location, mRNA translation and stability of mature mRNAs. Forms hnRNP particles with at least 20 other different hnRNP and heterogeneous nuclear RNA in the nucleus. Involved in transport of specific mRNAs to the cytoplasm in oligodendrocytes and neurons: acts by specifically recognizing and binding the A2RE (21 nucleotide hnRNP A2 response element) or the A2RE11 (derivative 11 nucleotide oligonucleotide) sequence motifs present on some mRNAs, and promotes their transport to the cytoplasm. Specifically binds single-stranded telomeric DNA sequences, protecting telomeric DNA repeat against endonuclease digestion. Also binds other RNA molecules, such as primary miRNA (pri-miRNAs): acts as a nuclear 'reader' of the N6-methyladenosine (m6A) mark by specifically recognizing and binding a subset of nuclear m6A-containing pri-miRNAs. Binding to m6A-containing pri-miRNAs promotes pri-miRNA processing by enhancing binding of DGCR8 to pri-miRNA transcripts. Involved in miRNA sorting into exosomes following sumoylation, possibly by binding (m6A)-containing pre-miRNAs. Acts as a regulator of efficiency of mRNA splicing, possibly by binding to m6A-containing pre-mRNAs. |
Source : | E. coli |
Species : | Mouse |
Tag : | His&SUMO |
Form : | Tris-based buffer,50% glycerol |
Molecular Mass : | 53.4 kDa |
Protein length : | 1-353 aa |
AA Sequence : | MEKTLETVPLERKKREKEQFRKLFI GGLSFETTEESLRNYYEQWGKLTDC VVMRDPASKRSRGFGFVTFSSMAEV DAAMAARPHSIDGRVVEPKRAVARE ESGKPGAHVTVKKLFVGGIKEDTEE HHLRDYFEEYGKIDTIEIITDRQSG KKRGFGFVTFDDHDPVDKIVLQKYH TINGHNAEVRKALSRQEMQEVQSSR SGRGGNFGFGDSRGGGGNFGPGPGS NFRGGSDGYGSGRGFGDGYNGYGGG PGGGNFGGSPGYGGGRGGYGGGGPG YGNQGGGYGGGYDNYGGGNYGSGSY NDFGNYNQQPSNYGPMKSGNFGGSR NMGGPYGGGNYGPGGSGGSGGYGGR SRY |
Purity : | > 90% as determined by SDS-PAGE. |
Notes : | Repeated freezing and thawing is not recommended. Store working aliquots at 4 centigrade for up to one week. |
Storage : | The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself. Generally, the shelf life of liquid form is 6 months at -20 centigrade/-80 centigrade. The shelf life of lyophilized form is 12 months at -20 centigrade/-80 centigrade. |
Concentration : | A hardcopy of COA will be sent along with the products. Please refer to it for detailed information. |
Gene Name : | Hnrnpa2b1 heterogeneous nuclear ribonucleoprotein A2/B1 [ Mus musculus ] |
Official Symbol : | HNRNPA2B1 |
Synonyms : | HNRNPA2B1; hnRNP A2/B1; hnRNP A2 / hnRNP B1; Hnrpa2; hnrnp-A; Hnrpa2b1; 9130414A06Rik; |
Gene ID : | 53379 |
mRNA Refseq : | NM_016806 |
Protein Refseq : | NP_058086 |
UniProt ID : | O88569 |
Products Types
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HNRNPA2B1-4911H | Recombinant Human HNRNPA2B1 Protein, GST-tagged | +Inquiry |
◆ Lysates | ||
HNRNPA2B1-334HCL | Recombinant Human HNRNPA2B1 lysate | +Inquiry |
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Not For Human Consumption!
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Write a reviewTop-notch analysis, a critical component of our research.
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Q&As (7)
Ask a questionIt influences mRNA splicing, affecting transcript diversity.
Genetic mutations in HNRNPA2B1 impact RNA splicing and processing.
HNRNPA2B1 is key for RNA processing and metabolism.
HNRNPA2B1 works with RNA-binding proteins to manage RNA regulation.
Altered HNRNPA2B1 activity is linked to neurodegenerative conditions.
HNRNPA2B1 regulates gene expression at the RNA level.
Targeting HNRNPA2B1 could treat RNA processing-related diseases.
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