Please ensure Javascript is enabled for purposes of website accessibility
Home / Products / Recombinant Protein / Other Proteins

Recombinant Human NUP133 Protein, N-His

Catalog #:   YHJ29501 Specific References (50) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: Q8WUM0
Protein length: Asp899-Asp1091
Overview

Catalog No.

YHJ29501

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Asp899-Asp1091

Predicted molecular weight

24.68 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

Q8WUM0

Applications

ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress

Form

Lyophilized

Storage buffer

Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.

Reconstitution

Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.

Shipping

In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Alternative Names

Nuclear pore complex protein Nup133, Nucleoporin Nup133, 133 kDa nucleoporin, NUP133

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human NUP133 protein
References

Nucleoporins cooperate with Polycomb silencers to promote transcriptional repression and repair at DNA double-strand breaks., PMID:40440073

Novel biallelic NUP107 variants affect the nuclear pore complex and expand the clinical spectrum to include brain malformations., PMID:40350250

Loss of Nup160 dysregulates Cdc42 in the podocytes of podocyte-specific Nup160 knockout mice., PMID:40298220

Nuclear pores safeguard the integrity of the nuclear envelope., PMID:40205196

Genetic and clinical spectrum of steroid-resistant nephrotic syndrome with nuclear pore gene mutation., PMID:39814977

The nucleoporin Nup153 is the anchor for Kif1a during basal nuclear migration in brain progenitor cells., PMID:39666457

Nucleoporin-associated steroid-resistant nephrotic syndrome., PMID:39331077

Nucleoporins cooperate with Polycomb silencers to promote transcriptional repression and repair at DNA double strand breaks., PMID:39070640

Mutations in nuclear pore complex promote osmotolerance in Arabidopsis by suppressing the nuclear translocation of ACQOS and its osmotically induced immunity., PMID:38318497

Nuclear pore complex proteins are involved in centromere distribution., PMID:38318384

The role of the FSGS disease gene product and nuclear pore protein NUP205 in regulating nuclear localization and activity of transcriptional regulators YAP and TAZ., PMID:37565816

Identification of novel nuclear pore complex associated proteins in esophageal carcinoma by an integrated bioinformatics analysis., PMID:37504972

Y-complex nucleoporins independently contribute to nuclear pore assembly and gene regulation in neuronal progenitors., PMID:37305998

Distinct domains in Ndc1 mediate its interaction with the Nup84 complex and the nuclear membrane., PMID:37154843

Steroid-resistant nephrotic syndrome caused by nuclear pore gene NUP133 variation., PMID:37041680

Diagnosis delay a family of Galloway-Mowat Syndrome caused by a classical splicing mutation of Lage3., PMID:36755238

A nuclear pore complex-associated regulation of SUMOylation in meiosis., PMID:36562208

Comprehensive maturity of nuclear pore complexes regulates zygotic genome activation., PMID:36493774

Predicting Novel Drug Candidates for Pancreatic Neuroendocrine Tumors via Gene Signature Comparison and Connectivity Mapping., PMID:35508682

NUP133 Controls Nuclear Pore Assembly, Transcriptome Composition, and Cytoskeleton Regulation in Podocytes., PMID:35455939

The endophilin curvature-sensitive motif requires electrostatic guidance to recycle synaptic vesicles in vivo., PMID:35303431

A labeling strategy with effective preservation of fluorophores for expansion single-molecule localization microscopy (Ex-SMLM)., PMID:34859796

Fetal Zone Steroids and Estrogen Show Sex Specific Effects on Oligodendrocyte Precursor Cells in Response to Oxidative Damage., PMID:34205405

Genetic interaction network has a very limited impact on the evolutionary trajectories in continuous culture-grown populations of yeast., PMID:34039270

Integrative Analysis of Transcriptome-Wide Association Study and mRNA Expression Profiles Identifies Candidate Genes Associated With Idiopathic Pulmonary Fibrosis., PMID:33362862

Yeast Nup84-Nup133 complex structure details flexibility and reveals conservation of the membrane anchoring ALPS motif., PMID:33247142

Nup133 and ERα mediate the differential effects of hyperoxia-induced damage in male and female OPCs., PMID:32844334

PinX1t, a Novel PinX1 Transcript Variant, Positively Regulates Cardiogenesis of Embryonic Stem Cells., PMID:32157956

Nuclear pore complex components have temperature-influenced roles in plant growth and immunity., PMID:32022936

One foot in the door: gene gating supports nuclear export of MYC mRNA., PMID:31875030

WNT signaling and AHCTF1 promote oncogenic MYC expression through super-enhancer-mediated gene gating., PMID:31784729

PPWD1 is associated with the occurrence of postmenopausal osteoporosis as determined by weighted gene co‑expression network analysis., PMID:31432133

Moderate Nucleoporin 133 deficiency leads to glomerular damage in zebrafish., PMID:30894603

Roles of Nup133, Nup153 and membrane fenestrations in assembly of the nuclear pore complex at the end of mitosis., PMID:30821042

Homozygous splicing mutation in NUP133 causes Galloway-Mowat syndrome., PMID:30427554

TMEM18: A Novel Prognostic Marker in Acute Myeloid Leukemia., PMID:30199869

Regulation of Cenp-F localization to nuclear pores and kinetochores., PMID:30198378

Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome., PMID:30179222

Analysis of RNA-Seq datasets reveals enrichment of tissue-specific splice variants for nuclear envelope proteins., PMID:29912636

Tracking the sarcoplasmic reticulum membrane voltage in muscle with a FRET biosensor., PMID:29899059

Nup133 Is Required for Proper Nuclear Pore Basket Assembly and Dynamics in Embryonic Stem Cells., PMID:29791854

Disentangling the molecular determinants for Cenp-F localization to nuclear pores and kinetochores., PMID:29632243

Mitotic nuclear pore complex segregation involves Nup2 in Aspergillus nidulans., PMID:28747316

Homozygous mutation in NUP107 leads to microcephaly with steroid-resistant nephrotic condition similar to Galloway-Mowat syndrome., PMID:28280135

Investigation of correlations between DNA methylation, suicidal behavior and aging., PMID:28276657

The development of a single molecule fluorescence standard and its application in estimating the stoichiometry of the nuclear pore complex., PMID:27613095

A nucleoporin that facilitates meiotic kinetochore reorganization., PMID:26727711

Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome., PMID:26411495

Crystal structure of human nuclear pore complex component NUP43., PMID:26391640

Membrane Curvature Sensing by Amphipathic Helices Is Modulated by the Surrounding Protein Backbone., PMID:26366573

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

Contact Information

Order: order@antibodysystem.com

Mail: support@antibodysystem.com

Distributor list

For research use only. Not for human or drug use.

Need help with your order?

Find out more about placing an order here

Recombinant Human NUP133 Protein, N-His [YHJ29501]
Terms of sale Website terms of use Cookie policy Privacy
Copyright © 2025 AntibodySystem SAS. All Rights Reserved.            All Products are for Research Use Only