Catalog No.
YHB86401
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Gly107-Asn345
Predicted molecular weight
29.45 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P00488
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
F13A1, Coagulation factor XIII A chain, Transglutaminase A chain, F13A, Coagulation factor XIIIa, Protein-glutamine gamma-glutamyltransferase A chain
Plasma Exosomal Proteomics Identifies Differentially Expressed Proteins as Biomarkers for Acute Myocardial Infarction., PMID:40305362
Novel Association of Thrombophilic PROS1, PROC and CPB2 Genes Polymorphisms with Recurrent Spontaneous Miscarriage Women in Jordan., PMID:40232193
Transcription factor RUNX1 regulates coagulation factor XIII-A (F13A1): decreased platelet-megakaryocyte F13A1 expression and clot contraction in RUNX1 haplodeficiency., PMID:39995753
Functional analysis of key members affecting egg production in the transglutaminase gene family in chickens., PMID:39813865
Transcription Factor RUNX1 Regulates Coagulation Factor XIII-A ( F13A1 ): Decreased Platelet-Megakaryocyte F13A1 Expression and Clot Contraction in RUNX1 Haplodeficiency., PMID:39763522
Factor XIII-A Transglutaminase Contributes to Neutrophil Extracellular Trap (NET)-mediated Fibrin(ogen) Network Formation and Crosslinking., PMID:39694058
M2 macrophage derived HMOX1 defines chronic rhinosinusitis with nasal polyps., PMID:39644500
Clinical Significance of Complement and Coagulation Cascades Genes for Patients With Acute Lymphoblastic Leukemia., PMID:39523585
Establishment of an Integrated Population Pharmacokinetic/ Pharmacodynamics Model of Apixaban in Chinese Healthy Population Adjusting for Key Genetic Variants., PMID:39449344
Cryo-EM structure of the human native plasma coagulation factor XIII complex., PMID:39447073
RUNX1 isoforms regulate RUNX1 and target genes differentially in platelets-megakaryocytes: association with clinical cardiovascular events., PMID:39181539
Identification of macrophage differentiation related genes and subtypes linking atherosclerosis plaque processing and metabolic syndrome via integrated bulk and single-cell sequence analysis., PMID:39130409
Activated platelets retain and protect most of their factor XIII-A cargo from proteolytic activation and degradation., PMID:39116293
Extraction of naturally occurring peptides versus the tryptic digestion of proteins from fetal versus adult bovine serum for LC-ESI-MS/MS., PMID:38461948
Epigenetic role of LINE-1 methylation and key genes in pregnancy maintenance., PMID:38332006
TGFβ macrophage reprogramming: a new dimension of macrophage plasticity., PMID:38197509
Relapsed/Refractory Peripheral T-Cell Lymphoma-Associated Hemophagocytic Lymphohistiocytosis With UNC13D and CD27 Germline Mutations., PMID:38183241
Large-scale functional inference for skin-expressing lncRNAs using expression and sequence information., PMID:38131377
Comprehensive analyses for the coagulation and macrophage-related genes to reveal their joint roles in the prognosis and immunotherapy of lung adenocarcinoma patients., PMID:38022584
Diagnostic biomarker for type 2 diabetic peripheral neuropathy via comprehensive bioinformatics analysis., PMID:38018513
Immune-related signature of periodontitis and Alzheimer's disease linkage., PMID:37849501
Discovery of plasma proteins associated with ventricular fibrillation during first ST-elevation myocardial infarction via proteomics., PMID:37811694
Unraveling dynamic interactions between tumor-associated macrophages and consensus molecular subtypes in colorectal cancer: An integrative analysis of single-cell and bulk RNA transcriptome., PMID:37662758
TGF-β uncouples glycolysis and inflammation in macrophages and controls survival during sepsis., PMID:37552767
Transglutaminases are oncogenic biomarkers in human cancers and therapeutic targeting of TGM2 blocks chemoresistance and macrophage infiltration in pancreatic cancer., PMID:37246171
IgE-binding monocytes upregulate the coagulation cascade in allergic horses., PMID:37193769
An Exploratory Study Using Next-Generation Sequencing to Identify Prothrombotic Variants in Patients with Cerebral Vein Thrombosis., PMID:37175682
Identification of a novel mutation in the factor XIII A subunit in a patient with inherited factor XIII deficiency., PMID:37059930
[Gene diagnosis of a family with coagulation factor ⅩⅢ deficiency caused by large deletion of F13A1 gene]., PMID:36987725
Identification of hub genes related to Duchenne muscular dystrophy by weighted gene co-expression network analysis., PMID:36596079
Genetic landscape in coagulation factor XIII associated defects - Advances in coagulation and beyond., PMID:36372609
Cysteine protease of Clonorchis sinensis alleviates DSS-induced colitis in mice., PMID:36084127
A novel F13A1 gene mutation (Arg208Pro) in a Chinese patient with factor XIII deficiency., PMID:35981255
Transient Platelet Dysfunction in Congenital Factor XIII Deficiency with Enhanced Thrombin Generation Potential., PMID:35975501
Maternal Thrombophilic and Hypofibrinolytic Genetic Variants in Idiopathic Recurrent Pregnancy Loss: a Continuing Mystery., PMID:35969362
[Analysis of genetic variant in a Chinese pedigree with hereditary factor VIII deficiency]., PMID:35810426
Exploring Diverse Coagulation Factor XIII Subunit Expression Datasets: A Bioinformatic Analysis., PMID:35563115
[Proteomics of serum exosomes in children in the acute stage of Kawasaki disease: a prospective study]., PMID:35527414
Transcriptome-based biomarker gene screening and evaluation of the extracellular fatty acid-binding protein (Ex-FABP) on immune and angiogenesis-related genes in chicken erythrocytes of tibial dyschondroplasia., PMID:35459093
Efficacy and Mechanism of Buyang Huanwu Decoction in Patients With Ischemic Heart Failure: A Randomized, Double-Blind, Placebo-Controlled Trial Combined With Proteomic Analysis., PMID:35370712
Dysfunctional Network and Mutation Genes of Hypertrophic Cardiomyopathy., PMID:35126952
Differential proteomic analysis demonstrates follicle fluid participate immune reaction and protein translation in yak., PMID:35031034
Exome-Sequencing Identifies Novel Genes Associated with Recurrent Pregnancy Loss in a Chinese Cohort., PMID:34925444
Platelet Phenotype Analysis of COVID-19 Patients Reveals Progressive Changes in the Activation of Integrin αIIbβ3, F13A1, the SARS-CoV-2 Target EIF4A1 and Annexin A5., PMID:34859078
Serum peptidome: diagnostic window into pathogenic processes following occupational exposure to carbon nanomaterials., PMID:34711247
Systematic proteomics analysis of lysine acetylation reveals critical features of placental proteins in pregnant women with preeclampsia., PMID:34697885
The human type 2 diabetes-specific visceral adipose tissue proteome and transcriptome in obesity., PMID:34462518
Cis-Segregation of c.1171C>T Stop Codon (p.R391*) in SERPINC1 Gene and c.1691G>A Transition (p.R506Q) in F5 Gene and Selected GWAS Multilocus Approach in Inherited Thrombophilia., PMID:34207366
Alterations of the Platelet Proteome in Lung Cancer: Accelerated F13A1 and ER Processing as New Actors in Hypercoagulability., PMID:34066760
Does iron overload in metabolic syndrome affect macrophage profile? A case control study., PMID:34022567
For research use only. Not for human or drug use.
