Full Product Name
GLE1 antibody
Product Gene Name
anti-GLE1 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Purity/Purification
Purified by antigen-affinity chromatography.
Form/Format
Supplied in 0.1M Tris-buffered saline with 10% Glycerol (pH7.0). 0.01% Thimerosal was added as a preservative.
Immunogen Type
Recombinant protein
Immunogen Description
Recombinant protein fragment contain a sequence corresponding to a region within amino acids 414 and 656 of GLE1
Preparation and Storage
Store at -20 degree C for long term preservation (recommended). Store at 4 degree C for short term use.
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
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]
Product Categories/Family for anti-GLE1 antibody
Total protein Ab
Applications Tested/Suitable for anti-GLE1 antibody
Western Blot (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
Application Notes for anti-GLE1 antibody
Western blotting: 1:500-1:3000
Immunohistochemistry: 1:100-1:500
Immunofluorescence: 1:100-1:200
Testing Data of anti-GLE1 antibody
Sample (30 ug of whole cell lysate)A: HeLa 7.5% SDS PAGEPrimary antibody diluted at 1: 1000

Immunohistochemistry (IHC) of anti-GLE1 antibody
Immunohistochemical analysis of paraffin-embedded Cal27 xenograft, using GLE1 antibody at 1: 500 dilution.

Immunofluorescence (IF) of anti-GLE1 antibody
Confocal immunofluorescence analysis (Olympus FV10i) of paraformaldehyde-fixed HeLa, using GLE1 antibody (Green) at 1: 500 dilution and alpha-tubulin antibody (Red) at 1: 2500.

NCBI/Uniprot data below describe general gene information for GLE1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001490
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NCBI GenBank Nucleotide #
NM_001499.2
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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 2
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: extracellular space; membrane; cytoplasm; plasma membrane; nuclear pore
Molecular Function: identical protein binding; protein binding
Biological Process: protein transport; poly(A)+ mRNA export from nucleus; mRNA export from nucleus
Disease: Lethal Arthrogryposis With Anterior Horn Cell Disease; Lethal Congenital Contracture Syndrome 1
Research Articles on GLE1
1. Lethal congenital contracture syndrome 1 and lethal arthrogryposis with anterior horn cell disease are associated with defective Gle1 function during the export of mRNA. [review]
Precautions
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