Catalog No.
YHF11501
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Asp38-His350
Predicted molecular weight
62.31 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P55268
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
S-laminin subunit beta, Laminin-9 subunit beta, Laminin B1s chain, Laminin-14 subunit beta, LAMS, Laminin-15 subunit beta, Laminin-11 subunit beta, Laminin-7 subunit beta, Laminin-4 subunit beta, S-LAM beta, LAMB2, Laminin subunit beta-2, Laminin-3 subunit beta, laminin 3, laminin 121, S laminin, laminin 4, laminin 221, S merosin, laminin 7, laminin 321, KS laminin, laminin 9, laminin 421, laminin 11, laminin 521, laminin-13, laminin-323, laminin-14, laminin-423, laminin-15, laminin-523
A spatially resolved transcriptome landscape during thyroid cancer progression., PMID:40157360
Urine Measurements of the Renin-Angiotensin System-Regulated Proteins Predict Death and Graft Loss in Kidney Transplant Recipients Enrolled in a Ramipril versus Placebo Randomized Controlled Trial., PMID:40111290
Candidate Genetic Modifiers in Alport Syndrome: A Case Series., PMID:40003707
Analysis of Alzheimer's disease associated deleterious non-synonymous single nucleotide polymorphisms and their impacts on protein structure and function by performing in-silico methods., PMID:39589570
Reconstruction of the Hepatic Microenvironment and Pathological Changes Underlying Type II Diabetes through Single-Cell RNA Sequencing., PMID:39494341
Machine learning model base on metabolomics and proteomics to predict cognitive impairment in Parkinson's disease., PMID:39394257
Laminin Beta 2 Is Localized at the Sites of Blood-Brain Barrier and Its Disruption Is Associated With Increased Vascular Permeability, Histochemical, and Transcriptomic Study., PMID:39340425
Overexpression of SLC2A1, ALDOC, and PFKFB4 in the glycolysis pathway drives strong drug resistance in 3D HeLa tumor cell spheroids., PMID:39295558
Hypoxia-induced LAMB2-enriched extracellular vesicles promote peritoneal metastasis in gastric cancer via the ROCK1-CAV1-Rab11 axis., PMID:39138263
Extracellular Matrix Protein Signatures of the Outer and Inner Zones of the Rat Adrenal Cortex., PMID:39018382
[Clinical and bioinformatics analysis of the relationship between LAMA3 DNA methylation expression and platinum resistance and prognosis in epithelial ovarian cancer]., PMID:38951081
Identification of established and novel extracellular matrix components in glioblastoma as targets for angiogenesis and prognosis., PMID:38775886
Expanding the spectrum of LAMB2: Pierson syndrome associated with neuromuscular junction disorder in two patients., PMID:38723581
Systematic identification of key basement membrane related genes as potential new biomarkers in Alzheimer's disease., PMID:38154381
Schwann Cells Do Not Promote Myogenic Differentiation in the EPI Loop Model., PMID:38063005
LAMB2 gene: broad clinical spectrum in Pierson syndrome., PMID:38038886
Congenital nephrotic syndrome with diffuse mesangial sclerosis caused by compound heterozygous mutation in LAMA5 gene., PMID:37985485
New Insights on Sperm Function in Male Infertility of Unknown Origin: A Multimodal Approach., PMID:37892144
Phenotype, genotype, and clinical outcome of Taiwanese with congenital nephrotic syndrome., PMID:37845138
Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease., PMID:37705905
Alterations in ileal transcriptomics during an intestinal barrier challenge in lactating Holstein cows fed a Saccharomyces cerevisiae fermentation product identify potential regulatory processes., PMID:37616596
Ocular manifestations of the genetic causes of focal and segmental glomerulosclerosis., PMID:37578539
A comparison of the ocular features in Pierson and Alport syndrome: a case report and literature review., PMID:37537573
Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome., PMID:37204080
Integrated proteome sequencing, bulk RNA sequencing and single-cell RNA sequencing to identify potential biomarkers in different grades of intervertebral disc degeneration., PMID:37009470
In-depth proteomic signature of parathyroid carcinoma., PMID:36995894
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review., PMID:36835142
Genomic signatures underlying the oogenesis of the ectoparasitic mite Varroa destructor on its new host Apis mellifera., PMID:36725182
Defining the altered glycoproteomic space of the early secretory pathway by class I mannosidase pharmacological inhibition., PMID:36699698
Transcriptomic and proteomic characteristics of the di(2-ethylhexyl) phthalate-induced sperm dna damage mouse model., PMID:36356568
Basigin is necessary for normal decidualization of human uterine stromal cells., PMID:36303457
Proteomics and liquid biopsy characterization of human EMT-related metastasis in colorectal cancer., PMID:36249004
Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa., PMID:35920919
Protein Network Analysis of Whole Exome Sequencing of Severe Preeclampsia., PMID:35719905
Key Genes Identified in Nonsyndromic Microtia by the Analysis of Transcriptomics and Proteomics., PMID:35647449
Astrocytes promote the proliferation of oligodendrocyte precursor cells through connexin 47-mediated LAMB2 secretion in exosomes., PMID:35596050
Heterozygous laminin β2 mutation in C3 glomerulopathy., PMID:35532722
Congenital nephrotic syndrome., PMID:34983935
A novel model of nephrotic syndrome results from a point mutation in Lama5 and is modified by genetic background., PMID:34774562
Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome., PMID:34546508
Immune checkpoint blockade reprograms systemic immune landscape and tumor microenvironment in obesity-associated breast cancer., PMID:34161764
Identification of Missense Extracellular Matrix Gene Variants in a Large Glaucoma Pedigree and Investigation of the N700S Thrombospondin-1 Variant in Normal and Glaucomatous Trabecular Meshwork Cells., PMID:34143713
Five-Year Follow-Up and Successful Kidney Transplantation in a Girl with a Severe Phenotype of Pierson Syndrome., PMID:34058744
LAMB2 novel variant c.2885-9 C>A affects RNA splicing in a minigene assay., PMID:33982833
Next-Generation Sequencing for Congenital Nephrotic Syndrome: A Multi-Center Cross-Sectional Study from India., PMID:33980730
Identification of seven tumor-educated platelets RNAs for cancer diagnosis., PMID:33955587
3D Mapping Reveals a Complex and Transient Interstitial Matrix During Murine Kidney Development., PMID:33875569
Association between the renin-angiotensin system and chronic lung allograft dysfunction., PMID:33863738
Neurological involvement in monogenic podocytopathies., PMID:33791874
For research use only. Not for human or drug use.
