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Mouse Anti-DIS3L2 Recombinant Antibody (D0940) (V2LY-0425-LY365)

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Summary

Host Animal
Mouse
Specificity
Human
Clone
D0940
Antibody Isotype
IgG1
Application
WB, IHC-P, FC, ELISA

Basic Information

Immunogen
Purified recombinant fragment of human DIS3L2 (aa27-250) expressed in E. Coli.
Host Species
Mouse
Specificity
Human
Antibody Isotype
IgG1
Clonality
Monoclonal Antibody
Application Notes
ApplicationNote
ELISA1:10,000
WB1:500-1:2,000
IHC1:200-1:1,000
FC1:200-1:400

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

Format
Liquid
Buffer
PBS
Preservative
Sodium Azide
Concentration
1 mg/ml
Purity
>95% as determined by analysis 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
DIS3 LIKE 3'-5' EXORIBONUCLEASE 2
Entrez Gene ID
UniProt ID
Function
3'-5'-exoribonuclease that specifically recognizes RNAs polyuridylated at their 3' end and mediates their degradation. Component of an exosome-independent RNA degradation pathway that mediates degradation of both mRNAs and miRNAs that have been polyuridylated by a terminal uridylyltransferase, such as ZCCHC11/TUT4. Mediates degradation of cytoplasmic mRNAs that have been deadenylated and subsequently uridylated at their 3'. Mediates degradation of uridylated pre-let-7 miRNAs, contributing to the maintenance of embryonic stem (ES) cells. Essential for correct mitosis, and negatively regulates cell proliferation.
Biological Process
Cell division Source: UniProtKB-KW
miRNA catabolic process Source: UniProtKB
Mitotic cell cycle Source: UniProtKB
Mitotic sister chromatid separation Source: UniProtKB
mRNA catabolic process Source: GO_Central
Negative regulation of cell population proliferation Source: UniProtKB
Nuclear-transcribed mRNA catabolic process, exonucleolytic Source: UniProtKB
Nuclear-transcribed mRNA catabolic process, exonucleolytic, 3'-5' Source: InterPro
Polyuridylation-dependent mRNA catabolic process Source: UniProtKB
Stem cell population maintenance Source: UniProtKB
Cellular Location
Cytoplasm; P-body
Involvement in disease
Perlman syndrome (PRLMNS):
An autosomal recessive congenital overgrowth syndrome. Affected children are large at birth, are hypotonic, and show organomegaly, characteristic facial dysmorphisms (inverted V-shaped upper lip, prominent forehead, deep-set eyes, broad and flat nasal bridge, and low-set ears), renal anomalies (nephromegaly and hydronephrosis), frequent neurodevelopmental delay, and high neonatal mortality. Perlman syndrome is associated with a high risk of Wilms tumor. Histologic examination of the kidneys in affected children shows frequent nephroblastomatosis, which is a precursor lesion for Wilms tumor.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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