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Recombinant Human LTBP2 Protein, N-His

Catalog #:   YHG89701 Specific References (50) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: Q14767
Protein length: Ser522-Thr814
Overview

Catalog No.

YHG89701

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Ser522-Thr814

Predicted molecular weight

33.80 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

Q14767

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.

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

LTBP-2, LTBP3, LTBP2, C14orf141, Latent-transforming growth factor beta-binding protein 2

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human LTBP2 protein
References

Inhibition of LTBP2 Suppresses High Glucose-Induced Proliferation, Fibrosis, and Inflammation in Glomerular Mesangial Cells by Disrupting the PI3K/Akt/NF-κB Pathway., PMID:40471644

LTBP2 variants in childhood glaucoma: Phenotypic expansion and clinical experience., PMID:40384769

A feasibility of computational drug screening for Fuchs endothelial corneal dystrophy., PMID:40287480

Comprehensive identification of dysregulated extracellular matrix molecules in the corneal endothelium of patients with Fuchs endothelial corneal dystrophy., PMID:40287463

Identification of unique biomarkers for proliferative diabetic retinopathy with tractional retinal detachment by proteomics profiling of vitreous humor., PMID:40251337

Targeting LTBP2 Derived from Cancer-Associated Fibroblasts Sensitizes Esophageal Squamous Cell Carcinoma to Chemotherapy., PMID:40245188

HIF-1α/LTBP2 axis activate HSCs to promote liver fibrosis by interacting with LOXL1 via the ERK pathway., PMID:40244455

Trbp inhibits cardiac fibrosis through TGF-β pathway-mediated cross-talk between cardiomyocytes and fibroblasts., PMID:40067137

Comprehensive bioinformatics analysis of hub genes in ischemic heart failure and atrial fibrillation., PMID:40066352

Unbiased CSF Proteomics in Patients With Idiopathic Normal Pressure Hydrocephalus to Identify Molecular Signatures and Candidate Biomarkers., PMID:39951680

Combined ADAMTS10 and ADAMTS17 inactivation exacerbates bone shortening and compromises extracellular matrix formation., PMID:39896540

Exome sequencing identifies existing and novel variants in a South African cohort presenting with anterior segment dysgenesis., PMID:39870121

Zonulopathies as Genetic Disorders of the Extracellular Matrix., PMID:39766898

LTBP2 silence suppresses glioblastoma proliferation and tumor growth of xenograft tumor mice through modulating JAK2/STAT2 signaling pathway., PMID:39752891

Dextromethorphan inhibits collagen and collagen-like cargo secretion to ameliorate lung fibrosis., PMID:39693409

Sodium Propionate Alleviates Atopic Dermatitis by Inhibiting Ferroptosis via Activation of LTBP2/FABP4 Signaling Pathway., PMID:39634285

Identification of fibrosis-associated biomarkers in heart failure and human cancers., PMID:39563337

Multi-modal analysis of human hepatic stellate cells identifies novel therapeutic targets for metabolic dysfunction-associated steatotic liver disease., PMID:39522884

Integrative analysis of whole genome bisulfite and transcriptome sequencing reveals the effect of sodium butyrate on DNA methylation in the differentiation of bovine skeletal muscle satellite cells., PMID:39521294

Trabecular Meshwork Abnormalities in a Model of Congenital Glaucoma Due to LTBP2 Mutation., PMID:39432401

Integrated bioinformatics analysis and experimental validation on malignant progression and immune cell infiltration of LTBP2 in gliomas., PMID:39390437

Potential Involvements of Cilia-Centrosomal Genes in Primary Congenital Glaucoma., PMID:39337513

Alterations in anterior lens capsule structure and LTBP-2 expression in primary angle-closure glaucoma., PMID:39317460

LTBP2 down-regulated FGF2 to repress vascular smooth muscle cell proliferation and vascular remodeling in a rat model of intracranial aneurysm., PMID:39288883

Targeted next-generation sequencing reveals the genetic mechanism of Chinese Marfan syndrome cohort with ocular manifestation., PMID:38958168

Matrisome Transcriptome Dynamics during Tissue Aging., PMID:38792614

Genotype-phenotype profile of global ASPH-associated ectopia lentis and clinical findings from a Chinese cohort., PMID:38788814

Autosomal Dominant Weill-Marchesani-Like Syndrome in a Chinese Family due to Novel Haplotypic Mutations in LTBP2., PMID:38772353

Exploring the Genetic Landscape of Childhood Glaucoma., PMID:38671671

Targeted plasma proteomic analysis uncovers a high-performance biomarker panel for early diagnosis of gastric cancer., PMID:38631604

Looking through the Glass: Microspherophakia with LTBP2 Mutation in Siblings., PMID:38613564

LTBP2 regulates cisplatin resistance in GC cells via activation of the NF-κB2/BCL3 pathway., PMID:38577985

A novel LTBP2 gene variant in a Turkish family with juvenile-onset open-angle glaucoma., PMID:38557215

Novel compound heterozygous variants in LTBP2 associated with relative anterior microphthalmos., PMID:38545692

Whole-Genome Resequencing of Ujimqin Sheep Identifies Genes Associated with Vertebral Number., PMID:38473062

SGLT2i improves kidney senescence by down-regulating the expression of LTBP2 in SAMP8 mice., PMID:38454800

Plasma proteomic profiles predict future dementia in healthy adults., PMID:38347190

Identification and phenotypic analysis of novel LTBP2 mutations in a Chinese cohort with congenital ectopia lentis., PMID:38222456

Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 Families., PMID:38190127

In vivo identification of angle dysgenesis and its relation to genetic markers associated with glaucoma using artificial intelligence., PMID:38146977

Proteomic and Phosphoproteomic Analysis of Right Ventricular Hypertrophy in the Pulmonary Hypertension Rat Model., PMID:38015796

Plasma LTBP2 as a potential biomarker in differential diagnosis of connective tissue disease-associated interstitial lung disease and idiopathic pulmonary fibrosis: a pilot study., PMID:37864077

Genome-wide association study using a single-step approach for teat number in Duroc, Landrace and Yorkshire pigs in Korea., PMID:37814452

Weill-Marchesani syndrome: natural history and genotype-phenotype correlations from 18 news cases and review of literature., PMID:37734846

Multi-organ phenotypes in mice lacking latent TGFβ binding protein 2 (LTBP2)., PMID:37688792

circWHSC1: A circular RNA piece in the human cancer puzzle., PMID:37549517

Characteristics and genotype-phenotype correlations in ADAMTS17 mutation-related Weill-Marchesani syndrome., PMID:37506754

Exclusion of previously described variant in LTBP2 for primary glaucoma in Australian Burmese cats., PMID:37499110

Aqueous Humor TGF-β2 and Its Association With Intraocular Pressure in a Naturally Occurring Large Animal Model of Glaucoma., PMID:37459065

Curcumin relieves arecoline-induced oral submucous fibrosis via inhibiting the LTBP2/NF-κB axis., PMID:37382472

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

Contact Information

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Distributor list

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

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Recombinant Human LTBP2 Protein, N-His [YHG89701]
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