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AB160843

Recombinant Human MBNL2 protein

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(1 Publication)

Recombinant Human MBNL2 protein is a Human Full Length protein, in the 1 to 373 aa range, expressed in Wheat germ, suitable for ELISA, WB.

View Alternative Names

MBLL, MBLL39, MLP1, MBNL2, Muscleblind-like protein 2, Muscleblind-like protein 1, Muscleblind-like protein-like, Muscleblind-like protein-like 39

1 Images
SDS-PAGE - Recombinant Human MBNL2 protein (AB160843)
  • SDS-PAGE

Unknown

SDS-PAGE - Recombinant Human MBNL2 protein (AB160843)

ab160843 on a 12.5% SDS-PAGE stained with Coomassie Blue.

Key facts

Expression system

Wheat germ

Tags

GST tag N-Terminus

Applications

WB, ELISA

applications

Biologically active

No

Accession

Q5VZF2

Animal free

No

Carrier free

No

Species

Human

Storage buffer

pH: 8 Constituents: 0.79% Tris HCl, 0.31% Glutathione

storage-buffer

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "ELISA": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "WB": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

Sequence info

[{"sequence":"MALNVAPVRDTKWLTLEVCRQFQRGTCSRSDEECKFAHPPKSCQVENGRVIACFDSLKGRCSRENCKYLHPPTHLKTQLEINGRNNLIQQKTAAAMLAQQMQFMFPGTPLHPVPTFPVGPAIGTNTAISFAPYLAPVTPGVGLVPTEILPTTPVIVPGSPPVTVPGSTATQKLLRTDKLEVCREFQRGNCARGETDCRFAHPADSTMIDTSDNTVTVCMDYIKGRCMREKCKYFHPPAHLQAKIKAAQHQANQAAVAAQAAAAAATVMAFPPGALHPLPKRQALEKSNGTSAVFNPSVLHYQQALTSAQLQQHAAFIPTGSVLCMTPATSIDNSEIISRNGMECQESALRITKHCYCTYYPVSSSIELPQTAC","proteinLength":"Full Length","predictedMolecularWeight":null,"actualMolecularWeight":null,"aminoAcidEnd":373,"aminoAcidStart":1,"nature":"Recombinant","expressionSystem":"Wheat germ","accessionNumber":"Q5VZF2","tags":[{"tag":"GST","terminus":"N-Terminus"}]}]

Properties and storage information

Shipped at conditions
Dry Ice
Appropriate short-term storage conditions
-80°C
Appropriate long-term storage conditions
-80°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle
False

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Muscleblind-like 2 (MBNL2) is an RNA-binding protein important for alternative splicing regulation with a mass approximately 39 kDa. Scientists also call it MBNL2. It is a member of the muscleblind-like protein family and displays extensive expression in skeletal muscle heart and brain tissues. MBNL2 contains four zinc finger domains typical for nucleic acid binding and interacts with pre-mRNA to influence splicing stability and translation processes. This interaction contributes to the regulation of diverse cellular activities.
Biological function summary

MBNL2 plays significant roles in the control of RNA splicing editing and transport. It does not work alone but often operates as part of a larger protein complex. The protein influences post-transcriptional gene expression and is essential for maintaining the proper isoform expression of various target proteins. This regulation affects development differentiation and function of muscle and neuronal tissues. MBNL2 serves as an important player in adjusting splicing patterns in response to cellular signals and stresses impacting the cell's adaptability and function.

Pathways

MBNL2 is intimately involved in the myotonic dystrophy splicing pathway affecting muscle and neuron function. It has a functional relationship with other muscleblind-like proteins such as MBNL1. These proteins collectively collaborate to regulate exon inclusion and exclusion in response to physiological changes. Furthermore MBNL2 participates in the circadian rhythm pathway influencing how cells adapt to daily environmental variations. It modulates the expression and processing of transcripts central to maintaining circadian clock accuracy and stability.

Dysfunction of MBNL2 associates with myotonic dystrophy type 1 (DM1) where abnormal repeats in RNA bind to the protein sequestering it away from normal splicing targets. This sequestration results in mis-splicing of many pre-mRNAs leading to symptoms linked with the disease. In DM1 MBNL2 works dynamically with MBNL1 to maintain splicing patterns and disruptions in their function cause overlapping yet distinct disease phenotypes. Additionally improper regulation of MBNL2 also connects to certain neurodegenerative conditions where alternative splicing errors contribute to pathology.

Specifications

Form

Liquid

General info

Function

Mediates pre-mRNA alternative splicing regulation. Acts either as activator or repressor of splicing on specific pre-mRNA targets. Inhibits cardiac troponin-T (TNNT2) pre-mRNA exon inclusion but induces insulin receptor (IR) pre-mRNA exon inclusion in muscle. Antagonizes the alternative splicing activity pattern of CELF proteins. RNA-binding protein that binds to 5'ACACCC-3' core sequence, termed zipcode, within the 3'UTR of ITGA3. Binds to CUG triplet repeat expansion in myotonic dystrophy muscle cells by sequestering the target RNAs. Together with RNA binding proteins RBPMS and RBFOX2, activates vascular smooth muscle cells alternative splicing events (By similarity). Regulates NCOR2 alternative splicing (By similarity). Seems to regulate expression and localization of ITGA3 by transporting it from the nucleus to cytoplasm at adhesion plaques. May play a role in myotonic dystrophy pathophysiology (DM).

Sequence similarities

Belongs to the muscleblind family.

Subcellular localisation

Nucleus

Product protocols

Target data

Mediates pre-mRNA alternative splicing regulation. Acts either as activator or repressor of splicing on specific pre-mRNA targets. Inhibits cardiac troponin-T (TNNT2) pre-mRNA exon inclusion but induces insulin receptor (IR) pre-mRNA exon inclusion in muscle. Antagonizes the alternative splicing activity pattern of CELF proteins. RNA-binding protein that binds to 5'ACACCC-3' core sequence, termed zipcode, within the 3'UTR of ITGA3. Binds to CUG triplet repeat expansion in myotonic dystrophy muscle cells by sequestering the target RNAs. Together with RNA binding proteins RBPMS and RBFOX2, activates vascular smooth muscle cells alternative splicing events (By similarity). Regulates NCOR2 alternative splicing (By similarity). Seems to regulate expression and localization of ITGA3 by transporting it from the nucleus to cytoplasm at adhesion plaques. May play a role in myotonic dystrophy pathophysiology (DM).
See full target information MBNL2

Publications (1)

Recent publications for all applications. Explore the full list and refine your search

Investigative ophthalmology & visual science 60:3980-3991 PubMed31560764

2019

Quantitative Studies of Muscleblind Proteins and Their Interaction With TCF4 RNA Foci Support Involvement in the Mechanism of Fuchs' Dystrophy.

Applications

Unspecified application

Species

Unspecified reactive species

Ziye Rong,Jiaxin Hu,David R Corey,V Vinod Mootha
View all publications

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