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Recombinant Human LSM2 protein is a Human Full Length protein, in the 1 to 95 aa range, expressed in Escherichia coli, with >90% purity and suitable for SDS-PAGE, MS.

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Images

SDS-PAGE - Recombinant Human LSM2 protein (AB124544), expandable thumbnail

Key facts

Purity
>90% SDS-PAGE
Expression system
Escherichia coli
Tags
His tag N-Terminus
Applications
SDS-PAGE, MS
Biologically active
No

Amino acid sequence

M G S S H H H H H H S S G L V P R G S H M G S H M L F Y S F F K S L V G K D V V V E L K N D L S I C G T L H S V D Q Y L N I K L T D I S V T D P E K Y P H M L S V K N C F I R G S V V R Y V Q L P A D E V D T Q L L Q D A A R K E A L Q Q K Q

Reactivity data

Application
SDS-PAGE
Reactivity
Reacts
Dilution info
-
Notes

-

Application
MS
Reactivity
Reacts
Dilution info
-
Notes

-

Target data

Function

Plays a role in pre-mRNA splicing as component of the U4/U6-U5 tri-snRNP complex that is involved in spliceosome assembly, and as component of the precatalytic spliceosome (spliceosome B complex) (PubMed:28781166). The heptameric LSM2-8 complex binds specifically to the 3'-terminal U-tract of U6 snRNA (PubMed:10523320).

Alternative names

Recommended products

Recombinant Human LSM2 protein is a Human Full Length protein, in the 1 to 95 aa range, expressed in Escherichia coli, with >90% purity and suitable for SDS-PAGE, MS.

Key facts

Purity
>90% SDS-PAGE
Expression system
Escherichia coli
Applications
SDS-PAGE, MS
Accession
Q9Y333-1
Animal free
No
Species
Human
Concentration
Loading...
Storage buffer

pH: 8
Constituents: 40% Glycerol (glycerin, glycerine), 1.17% Sodium chloride, 0.32% Tris HCl, 0.08% (R*,R*)-1,4-Dimercaptobutan-2,3-diol

Sequence info

Amino acid sequence

M G S S H H H H H H S S G L V P R G S H M G S H M L F Y S F F K S L V G K D V V V E L K N D L S I C G T L H S V D Q Y L N I K L T D I S V T D P E K Y P H M L S V K N C F I R G S V V R Y V Q L P A D E V D T Q L L Q D A A R K E A L Q Q K Q
Accession
Q9Y333
Protein length
Full Length
Predicted molecular weight
13.4 kDa
Amino acids
1 to 95
Nature
Recombinant
Tags
His tag N-Terminus

Specifications

Form
Liquid
Additional notes

ab124544 is purified using conventional chromatography techniques.

General info

Function

Plays a role in pre-mRNA splicing as component of the U4/U6-U5 tri-snRNP complex that is involved in spliceosome assembly, and as component of the precatalytic spliceosome (spliceosome B complex) (PubMed:28781166). The heptameric LSM2-8 complex binds specifically to the 3'-terminal U-tract of U6 snRNA (PubMed:10523320).

Sequence similarities

Belongs to the snRNP Sm proteins family.

Subcellular localisation
Nucleus

Storage

Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary info

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

LSM2 also known as Like-Smith 2 is a protein involved in RNA processing and stabilization. It has a mass of approximately 14 kDa. This protein is mainly expressed in the cytoplasm and nucleus and its presence is critical in cells with active RNA metabolism. The structure of LSM2 enables it to participate in RNA decay and splicing pathways making it an important player in RNA regulation.

Biological function summary

Proteins coordinate complex molecular processes within cells. LSM2 is part of the Lsm1-7 complex which binds to the 3' ends of mRNA and facilitates mRNA decapping and decay. This complex supports RNA metabolism by modulating mRNA stability and is essential for proper cellular function and response to environmental changes.

Pathways

The functions of LSM2 integrate into RNA processing pathways like mRNA decay and splicing. In the mRNA decay pathway LSM2 through the Lsm1-7 complex works alongside decapping proteins to regulate mRNA turnover influencing gene expression levels. Additionally in splicing LSM2 influences the splicing machinery interacting with proteins like U6 snRNA ensuring accurate splicing of pre-mRNA.

Associated diseases and disorders

Researchers have linked abnormalities in LSM2 function to neurodegenerative diseases such as spinal muscular atrophy. Mutations or malfunctions in LSM2 disrupt RNA processing especially mRNA decay leading to improper gene expression. These disruptions can involve proteins like SMN (Survival Motor Neuron) highlighting LSM2's role in maintaining neuron integrity and function.

Product promise

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1 product image

  • SDS-PAGE - Recombinant Human LSM2 protein (ab124544), expandable thumbnail

    SDS-PAGE - Recombinant Human LSM2 protein (ab124544)

    15% SDS-PAGE analysis of 3 μg ab124544.

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Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

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