Full Product Name
GLE1 Antibody; Biotin conjugated
Product Synonym Names
Nucleoporin GLE1; hGLE1; GLE1-like protein; GLE1; GLE1L
Product Gene Name
anti-GLE1 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q53GS7
Purity/Purification
>95%,Protein G purified
Immunogen
Recombinant human Nucleoporin GLE1 protein
Storage Buffer
Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Santa Cruz Alternative
Potential replacement for Santa Cruz Biotechnology antibody catalog# sc-98363 / sc-74932 / sc-74934
Preparation and Storage
Shipped at 4 degree C. Upon delivery, aliquot and store at -20 degree C or -80 degree C.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of anti-GLE1 antibody 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
anti-GLE1 antibody
Required for the export of mRNAs containing poly(A) tails from the nucleus into the cytoplasm. May be involved in the terminal step of the mRNA transport through the nuclear pore complex (NPC).
Applications Tested/Suitable for anti-GLE1 antibody
ELISA (EIA)
NCBI/Uniprot data below describe general gene information for GLE1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001003722.1
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NCBI GenBank Nucleotide #
NM_001003722.1
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UniProt Primary Accession #
Q53GS7
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UniProt Secondary Accession #
O75458; Q53GT9; Q5VVU1; Q8NCP6; Q9UFL6[Other Products]
UniProt Related Accession #
Q53GS7[Other Products]
Molecular Weight
75,407 Da
NCBI Official Full Name
nucleoporin GLE1 isoform 1
NCBI Official Synonym Full Names
GLE1, RNA export mediator
NCBI Official Symbol
GLE1??[Similar Products]
NCBI Official Synonym Symbols
LCCS; GLE1L; LCCS1; hGLE1
??[Similar Products]
NCBI Protein Information
nucleoporin GLE1
UniProt Protein Name
Nucleoporin GLE1
UniProt Synonym Protein Names
GLE1-like protein
UniProt Gene Name
GLE1??[Similar Products]
UniProt Synonym Gene Names
GLE1L; hGLE1??[Similar Products]
UniProt Entry Name
GLE1_HUMAN
NCBI Summary for GLE1
This gene encodes a predicted 75-kDa polypeptide with high sequence and structure homology to yeast Gle1p, which is nuclear protein with a leucine-rich nuclear export sequence essential for poly(A)+RNA export. Inhibition of human GLE1L by microinjection of antibodies against GLE1L in HeLa cells resulted in inhibition of poly(A)+RNA export. Immunoflourescence studies show that GLE1L is localized at the nuclear pore complexes. This localization suggests that GLE1L may act at a terminal step in the export of mature RNA messages to the cytoplasm. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
UniProt Comments for GLE1
GLE1: Required for the export of mRNAs containing poly(A) tails from the nucleus into the cytoplasm. May be involved in the terminal step of the mRNA transport through the nuclear pore complex (NPC). Defects in GLE1 are the cause of lethal congenital contracture syndrome type 1 (LCCS1); also known as multiple contracture syndrome type Finnish. LCCS is an autosomal recessive disorder characterized by early fetal hydrops and akinesia, micrognatia, pulmonary hypoplasia, pterygia, multiple joint contractures, specific neuropathology with degeneration of anterior horn neurons and extreme skeletal muscle atrophy. LCCS1 leads to prenatal death. Defects in GLE1 are the cause of lethal arthrogryposis with anterior horn cell disease (LAAHD). LAAHD is characterized by fetal akinesia, arthrogryposis and motor neuron loss. LAADH fetus often survive delivery, but die early as a result of respiratory failure. Neuropathological findings resemble those of LCCS1, but are less severe. Belongs to the GLE1 family. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Nuclear export; Karyopherin
Chromosomal Location of Human Ortholog: 9q34.11
Cellular Component: cytoplasm; extracellular space; membrane; nuclear pore; plasma membrane
Molecular Function: identical protein binding; protein binding
Biological Process: mRNA export from nucleus; poly(A)+ mRNA export from nucleus; protein transport
Disease: Lethal Arthrogryposis With Anterior Horn Cell Disease; Lethal Congenital Contracture Syndrome 1
Research Articles on GLE1
1. Role for Gle1A during stress granule formation and translation regulation during environmental stress responses is examined.
Precautions
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Disclaimer
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