Catalog No.
YHC30201
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Val1103-Lys1366
Predicted molecular weight
31.99 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P08123
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
Collagen alpha-2(I) chain, COL1A2, Alpha-2 type I collagen
The Direct and Individual Transcriptional Function of the Human Homodimeric and Heterodimeric Basic Helix-Loop-Helix Transcription Factors E47 and Scleraxis., PMID:40512054
The Impact of Selected COL1A1 and COL1A2 Gene Polymorphisms on Bone Mineral Density and the Risk of Metabolic Diseases in Postmenopausal Women., PMID:40507792
Hepatic transcriptome profiling unveils candidate genes in cattle with liver abscesses under the influence of beef genetics in dairy cattle., PMID:40489480
Mast cell tryptase-PAR2 axis promotes ovarian fibrosis through RNF152-mediated stabilization of Bcl-xL., PMID:40474218
Transcriptome and proteome profile analysis of the regulation of chicken ovarian development., PMID:40466268
ECM remodeling by PDGFRβ+ dental pulp stem cells drives angiogenesis and pulp regeneration via integrin signaling., PMID:40462244
Splice‑site variant c.3531+1G>T in COL1A1 in a family with osteogenesis imperfecta., PMID:40444480
Candidate genes validation for intramuscular fat content of Nellore Cattle., PMID:40435528
Hair-follicle-associated pluripotent (HAP) stem-cell-sheet implantation accelerates cutaneous wound closure and suppresses scar formation in a mouse model., PMID:40432248
Exploring shared pathogenic mechanisms and biomarkers in hepatic fibrosis and inflammatory bowel disease through bioinformatics and machine learning., PMID:40421012
Peripheral Choroid/RPE/Sclera as a Shared Pathogenic Hub: Multi-Tissue Transcriptomic Profiling Identifies Common Differentially Expressed Genes in Age-Related Macular Degeneration and Alzheimer's Disease., PMID:40411685
Autophagic degradation of SQSTM1 enables fibroblast activation to accelerate wound healing., PMID:40400126
Stress exposure affects amyotrophic lateral sclerosis pathogenesis via PI3K/Akt and focal adhesion pathways: evidence from three experimental models., PMID:40399476
Col1a2oim/oim mice exhibit alterations in ossicular bone quality typical of osteogenesis imperfecta but no hearing loss., PMID:40398629
A diet-driven metabolic dysfunction-associated steatohepatitis (MASH) mouse model resembles the corresponding human disease., PMID:40392411
POSTN Silencing Ameliorates LL37-Induced Rosacea and Inhibits the JAK2/STAT3 and NF-κB Pathways., PMID:40387439
Osteogenesis imperfecta type V: About a clinical case., PMID:40379599
Transcriptome-Wide Analysis and Experimental Validation from FFPE Tissue Identifies Stage-Specific Gene Expression Profiles Differentiating Adenoma, Carcinoma In-Situ and Adenocarcinoma in Colorectal Cancer Progression., PMID:40362431
Active synthesis of type I collagen homotrimer in Dupuytren's fibrosis is unaffected by anti-TNF-α treatment., PMID:40337865
Combining ATAC-seq and RNA-seq reveals key genes for gonadal abnormalities in one-month-old XX-DSD pigs., PMID:40329180
Altered expression of collagen gene family members and its epigenetic background in equine Sarcoids., PMID:40288239
Investigation of Lactobacillus Probiotics Derived from Traditional Dairy Products in Eliciting Anti-Tumor Responses in Mouse Colorectal Cancer Model., PMID:40255226
iTRAQ-based quantitative proteomics reveals dysregulation of fibronectin 1 contributes to impaired endometrial decidualization in recurrent implantation failure., PMID:40187609
Overexpression of miR-192 in fibroblasts accelerates wound healing in diabetic rats: research article., PMID:40186269
Genetic landscape and phenotypic spectrum of osteogenesis imperfecta in the Kazakhstani pediatric population., PMID:40175636
Cold aerobic exercise mitigates NAFLD fibrosis through UBAP2L-regulated TGF-β/SMAD2 signaling., PMID:40163653
Free omental patch as the promising future for incisional hernia surgery: an experimental study in rat model., PMID:40145159
Whole exome sequencing of 80 cases of sporadic mitral valve prolapse reveals novel disease-associated genes and variants in a Southern Chinese population., PMID:40131712
Chemokine (C-C Motif) Ligand 2 Expressing Adventitial Fibroblast Expansion During Loeys-Dietz Syndrome Aortic Aneurysm Formation., PMID:40109260
Comprehensive analysis of the effects of P4ha1 and P4ha2 deletion on post-translational modifications of fibrillar collagens in mouse skin., PMID:40092628
Drug-likeness evaluation and inhibitory mechanism of the emodin derivative on cardiac fibrosis based on metastasis-associated protein 3., PMID:40083252
Seven Hub Genes Associated with Huntington's Disease and Diagnostic and Therapeutic Potentials Identified by Computational Biology., PMID:40059764
COL1A1 and COL1A2 Gene Variants Causing Osteogenesis Imperfecta in a Major Referral Center of India., PMID:40047057
EGFR influences the resistance to targeted therapy in BRAF V600E melanomas by regulating the ferroptosis process., PMID:40024937
Spatial transcriptomics reveals prognostically LYZ+ fibroblasts and colocalization with FN1+ macrophages in diffuse large B-cell lymphoma., PMID:39998673
Disrupted maxillofacial, cardiovascular, and nervous development in washc5 knockout Zebrafish: Insights into 3C syndrome., PMID:39988189
Registry-Based Frequency of Molecularly Confirmed Osteogenesis Imperfecta in a Swiss Cohort of Individuals With Connective Tissue Disorders., PMID:39957537
Genomic Profiling Uncovers a Broader Spectrum of Dermatofibrosarcoma Protuberans: Implications for Diagnosis and Therapy., PMID:39956270
Classical Ehlers-Danlos syndrome with cranio-cervical instability in an infant due to a novel COL5A1 gene mutation., PMID:39950632
Skin Telocyte Secretome as Conditioned Medium Prevents Profibrotic Differentiation of Skin Fibroblasts into Myofibroblasts., PMID:39941052
Proteomic profiling reveals biological processes and biomarkers involved in the pathogenesis of occult breast cancer., PMID:39930421
Identifying rare variants in genes related to bone phenotypes in a cohort of postmenopausal women., PMID:39915337
Diagnostic potential of CDK1 and STAT1 in acute kidney injury associated with gastrointestinal cancers: a bioinformatics-based study., PMID:39911265
Pleiotropic effects of a recessive Col1a2 mutation occurring in a mouse model of severe osteogenesis imperfecta., PMID:39908220
Lamellarin D Acts as an Inhibitor of Type I Collagen Production., PMID:39887929
LARP6 regulates the mRNA translation of fibrogenic genes in liver fibrosis., PMID:39868246
Micropillar-induced changes in cell nucleus morphology enhance bone regeneration by modulating the secretome., PMID:39866882
Enhanced ovarian FKBP51 expression is associated with ovarian aging: a molecular insight for age-related fertility in women., PMID:39837475
COL1A1, COL1A2, CHN1, and FN1 Promote Tumorogenesis and Act as Markers of Diagnosis and Survival in Gastric Cancer Patients., PMID:39812067
The genetics of non-syndromic dentinogenesis imperfecta: a systematic review., PMID:39806231
For research use only. Not for human or drug use.
