Product Name
MGC42174, Blocking Peptide
Full Product Name
MGC42174 Peptide - N-terminal region
Product Gene Name
MGC42174 blocking peptide
[Similar Products]
Product Synonym Gene Name
FAM6A; MGC42174; DIS3L2[Similar Products]
MGC42174 peptide (MBS3230637) is used for blocking the activity of MGC42174 antibody (MBS3205673)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q8IYB7
Form/Format
Lyophilized powder
Preparation and Storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Other Notes
Small volumes of MGC42174 blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
MGC42174 blocking peptide
The function remains unknown.
Product Categories/Family for MGC42174 blocking peptide
Peptide
Applications Tested/Suitable for MGC42174 blocking peptide
Immunohistochemistry (IHC), Western Blot (WB)
NCBI/Uniprot data below describe general gene information for MGC42174. It may not necessarily be applicable to this product.
NCBI Accession #
NP_689596
[Other Products]
NCBI GenBank Nucleotide #
NM_152383
[Other Products]
UniProt Primary Accession #
Q8IYB7
[Other Products]
UniProt Related Accession #
Q8IYB7[Other Products]
NCBI Official Full Name
DIS3-like exonuclease 2 isoform 1
NCBI Official Synonym Full Names
DIS3 like 3'-5' exoribonuclease 2
NCBI Official Symbol
DIS3L2 [Similar Products]
NCBI Official Synonym Symbols
FAM6A; PRLMNS; hDIS3L2
[Similar Products]
NCBI Protein Information
DIS3-like exonuclease 2
UniProt Protein Name
DIS3-like exonuclease 2
UniProt Gene Name
DIS3L2 [Similar Products]
UniProt Synonym Gene Names
hDIS3L2 [Similar Products]
UniProt Entry Name
DI3L2_HUMAN
NCBI Summary for MGC42174
The protein encoded by this gene is similar in sequence to 3'/5' exonucleolytic subunits of the RNA exosome. The exosome is a large multimeric ribonucleotide complex responsible for degrading various RNA substrates. Several transcript variants, some protein-coding and some not, have been found for this gene. [provided by RefSeq, Mar 2012]
UniProt Comments for MGC42174
DIS3L2: Ribonuclease that plays a critical role in RNA metabolism. It is essential for correct mitosis, and negatively regulates cell proliferation. Defects in DIS3L2 are the cause of 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. Belongs to the RNR ribonuclease family. 5 isoforms of the human protein are produced by alternative splicing.
Protein type: EC 3.1.13.-; Ribonuclease; Tumor suppressor
Chromosomal Location of Human Ortholog: 2q37.1
Cellular Component: cytoplasm; nuclear exosome (RNase complex); polysome
Molecular Function: 3'-5'-exoribonuclease activity; magnesium ion binding; poly(U) binding; protein binding; ribonuclease activity
Biological Process: cell division; mitosis; mitotic sister chromatid separation; mRNA catabolic process, exonucleolytic; negative regulation of cell proliferation; rRNA catabolic process; rRNA processing; stem cell maintenance
Disease: Perlman Syndrome
Research Articles on MGC42174
1. These findings suggest that sequestration of the exoribonucleases DIS3L2 and XRN1 to nuclear inclusions may be related to the pathogenesis of intranuclear inclusion body disease
Precautions
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Disclaimer
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