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Recombinant Human LMX1B Protein, N-His

Catalog #:   YHA96701 Specific References (50) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: O60663
Protein length: Cys56-Lys173
Overview

Catalog No.

YHA96701

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Cys56-Lys173

Predicted molecular weight

16.05 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

O60663

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

LIM/homeobox protein 1.2, LIM/homeobox protein LMX1B, LMX1B, LIM homeobox transcription factor 1-beta, LMX-1.2

Data Image
  • SDS-PAGE
    SDS-PAGE for Recombinant Human LMX1B protein
References

Identification of a novel missense variant in the LMX1B gene associated with nail-patella syndrome in a Chinese family., PMID:40421384

A novel variation in the LMX1B gene with nail-patella syndrome., PMID:40174274

LMX1B missense-perturbation of regulatory element footprints disrupts serotonergic forebrain axon arborization., PMID:40168115

LMX1B haploinsufficiency due to variants in the 5'UTR as a cause of Nail-Patella syndrome., PMID:39939609

AMPK Phosphorylates LMX1b to Regulate a Brainstem Neurogenic Network Important for Control of Breathing in Neonatal Mice., PMID:39796072

The molecular mechanism of Xiaoyaosan in treating major depressive disorder: Integrated analysis of DNA methylation and RNA sequencing of the arcuate nucleus in rats., PMID:39675591

Versican controlled by Lmx1b regulates hyaluronate density and hydration for semicircular canal morphogenesis., PMID:39651757

Molecular Ontology of the Nucleus of Solitary Tract., PMID:39629676

A multicenter study investigating the genetic analysis of childhood steroid-resistant nephrotic syndrome: Variants in COL4A5 may not be coincidental., PMID:39625990

Focal segmental glomerulosclerosis associated with undescribed mutation in the LMX1B gene., PMID:39490407

Genetic polymorphisms of LMX1B and MLXIP are associated with hip osteoarthritis in the Chinese population., PMID:39263770

Non-dialyzable uremic toxins and renal tubular cell damage in CKD patients: a systems biology approach., PMID:39123228

A Family With Nail-Patella Syndrome Caused by a Germline Mosaic Deletion of LMX1B., PMID:39038913

Versican controlled by Lmx1b regulates hyaluronate density and hydration for semicircular canal morphogenesis., PMID:38766227

Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene., PMID:38663984

Disfunction of dorsal raphe nucleus-hippocampus serotonergic-HTR3 transmission results in anxiety phenotype of Neuroplastin 65-deficient mice., PMID:38528118

Nail-patella syndrome with nephropathy in a de novo LMX1B mutation: triangular lunula of the thumb and lack of finger creases as clues., PMID:38478172

Case report: A novel R246L mutation in the LMX1B homeodomain causes isolated nephropathy in a large Chinese family., PMID:38457557

A deletion variant in LMX1B causing nail-patella syndrome in Japanese twins., PMID:38424113

The limb dorsoventral axis: Lmx1b's role in development, pathology, evolution, and regeneration., PMID:38288855

High throughput functional profiling of genes at intraocular pressure loci reveals distinct networks for glaucoma., PMID:38272457

In-depth analyses of lncRNA and circRNA expression in the hippocampus of LPS-induced AD mice by Byu d Mar 25., PMID:38051653

De novo enhancer deletion of LMX1B produces a mild nail-patella clinical phenotype., PMID:37899549

Identification of candidate genes and chemicals associated with osteoarthritis by transcriptome-wide association study and chemical-gene interaction analysis., PMID:37749624

ATG8 proteins are co-factors for human dopaminergic neuronal transcriptional control: implications for neuronal resilience in Parkinson disease., PMID:37312406

LC3B is a cofactor for LMX1B-mediated transcription of autophagy genes in dopaminergic neurons., PMID:37036692

ATG8-dependent LMX1B-autophagy crosstalk shapes human midbrain dopaminergic neuronal resilience., PMID:37014324

Prolonged Differentiation of Neuron-Astrocyte Co-Cultures Results in Emergence of Dopaminergic Neurons., PMID:36835019

Genes critical for development and differentiation of dopaminergic neurons are downregulated in Parkinson's disease., PMID:36820885

Derivation of the Immortalized Cell Line UM51-PrePodo-hTERT and Its Responsiveness to Angiotensin II and Activation of the RAAS Pathway., PMID:36766685

Enhancing Neurological Competence of Nanoencapsulated Cordyceps/Turmeric Extracts in Human Neuroblastoma SH-SY5Y Cells., PMID:36660588

Identification of ARMH4 and WIPF3 as human podocyte proteins with potential roles in immunomodulation and cytoskeletal dynamics., PMID:36649229

Failure of digit tip regeneration in the absence of Lmx1b suggests Lmx1b functions disparate from dorsoventral polarity., PMID:36641754

Targeted Methylation Profiling of Single Laser-Capture Microdissected Post-Mortem Brain Cells by Adapted Limiting Dilution Bisulfite Pyrosequencing (LDBSP)., PMID:36555213

Simultaneous kidney and pancreas transplantation in a patient with nail-patella syndrome and insulin-dependent diabetes., PMID:36434354

Role of Sonic Hedgehog Signaling Activation in the Prevention of Neurological Abnormalities Associated with Obsessive-Compulsive Disorder., PMID:36272053

Knockdown of LMX1B Suppressed Cell Apoptosis and Inflammatory Response in IL-1β-Induced Human Osteoarthritis Chondrocytes through NF-κB and NLRP3 Signal Pathway., PMID:36133743

Triphenyl phosphate disturbs placental tryptophan metabolism and induces neurobehavior abnormal in male offspring., PMID:36007322

Hippocampal DNA Methylation, Epigenetic Age, and Spatial Memory Performance in Young and Old Rats., PMID:35917578

LMX1B Activated Circular RNA GFRA1 Modulates the Tumorigenic Properties and Immune Escape of Prostate Cancer., PMID:35832649

Case Report: Inversion of LMX1B - A Novel Cause of Nail-Patella Syndrome in a Swedish Family and a Longtime Follow-Up., PMID:35769074

A novel LMX1B mutation: nail-patella syndrome manifesting with isolated nail disorders., PMID:35643888

Transcriptional preservation of serotonergic connectivity may shed light on neurodegeneration., PMID:35624030

Transcription Factor Lmx1b Negatively Regulates Osteoblast Differentiation and Bone Formation., PMID:35563615

The WNT7A/WNT7B/GPR124/RECK signaling module plays an essential role in mammalian limb development., PMID:35552394

Reorganization of postmitotic neuronal chromatin accessibility for maturation of serotonergic identity., PMID:35471146

An adult-stage transcriptional program for survival of serotonergic connectivity., PMID:35443166

Maternal Herpesviridae infection during pregnancy alters midbrain dopaminergic signatures in adult offspring., PMID:35417751

hsa-miR-206b Involves in the Development of Papillary Thyroid Carcinoma via Targeting LMX1B., PMID:35342753

Lhx2 in germ cells suppresses endothelial cell migration in the developing ovary., PMID:35337816

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

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

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Recombinant Human LMX1B Protein, N-His [YHA96701]
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