Mouse Anti-GLE1 Recombinant Antibody (CBLG1-3174) (V2LY-1225-LY1444)

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Basic Information

Host Animal
Mouse
Clone
CBLG1-3174
Application
WB, IP, IF, ELISA
Immunogen
Amino acids 399-698 mapping at the C-terminus of human Gle1.
Host Species
Mouse
Specificity
Human, Mouse, Rat
Antibody Isotype
IgG1, λ
Clonality
Monoclonal
Application Notes
ApplicationNote
ELISA1:100-1:1,000
WB1:100-1:1,000
IP1-2 µg per 100-500 µg of total protein (1 ml of cell lysate)
IF(ICC)1:50-1:500

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

Format
Liquid
Buffer
PBS, gelatin
Preservative
Sodium azide
Concentration
0.2 mg/ml
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.
More Infomation

Target

Full Name
GLE1 RNA export mediator homolog (yeast)
Entrez Gene ID
UniProt ID
Function
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).
Biological Process
mRNA export from nucleus Source: GO_Central
Poly(A)+ mRNA export from nucleus Source: InterPro
Protein transport Source: UniProtKB-KW
Regulation of translational initiation Source: GO_Central
Regulation of translational termination Source: GO_Central
Cellular Location
Cytoplasm; Nucleus. Shuttles between the nucleus and the cytoplasm (PubMed:12668658). Shuttling is essential for its mRNA export function (PubMed:12668658).
Isoform 1: Nuclear pore complex; Cytoplasm. Shuttles between the nucleus and the cytoplasm (PubMed:12668658). In the nucleus, isoform 1 localizes to the nuclear pore complex and nuclear envelope (PubMed:12668658). Shuttling is essential for its mRNA export function (PubMed:12668658).
Involvement in disease
Lethal congenital contracture syndrome 1 (LCCS1):
A form of lethal congenital contracture syndrome, an autosomal recessive disorder characterized by degeneration of anterior horn neurons, extreme skeletal muscle atrophy, and congenital non-progressive joint contractures (arthrogryposis). The contractures can involve the upper or lower limbs and/or the vertebral column, leading to various degrees of flexion or extension limitations evident at birth. LCCS1 patients manifest early fetal hydrops and akinesia, micrognathia, pulmonary hypoplasia, pterygia, and multiple joint contractures. It leads to prenatal death.
Congenital arthrogryposis with anterior horn cell disease (CAAHD):
An autosomal recessive disorder characterized by fetal akinesia, arthrogryposis and motor neuron loss. The fetus often survives delivery, but dies early as a result of respiratory failure. Neuropathological findings resemble those of lethal congenital contracture syndrome type 1, but are less severe.
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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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