Catalog No.
YHC14501
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Lys333-Gln650
Predicted molecular weight
38.42 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P05160
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
Coagulation factor XIII B chain, Fibrin-stabilizing factor B subunit, Protein-glutamine gamma-glutamyltransferase B chain, Transglutaminase B chain, F13B
Acute mountain sickness prediction: a concerto of multidimensional phenotypic data and machine learning strategies in the framework of predictive, preventive, and personalized medicine., PMID:40438497
Protective Vaccination of Mice Against Blood-Stage Malaria Impacts Hepatic Expression of Genes Encoding Acute-Phase Proteins and IL-6 Family Members., PMID:40243929
Identifcation of candidate biomarkers for polyarteritis nodosa using data-independent acquisition mass spectrometry., PMID:39959243
Factor XIII Deficiency: Laboratory, Molecular, and Clinical Aspects., PMID:39613144
F13B regulates angiogenesis and tumor progression in hepatocellular carcinoma via the HIF-1α/VEGF pathway., PMID:39319846
Serum Biomarkers of Vascular Involvement in Childhood Uveitis., PMID:38573655
Epigenetic role of LINE-1 methylation and key genes in pregnancy maintenance., PMID:38332006
Reciprocal stabilization of coagulation factor XIII-A and -B subunits is a determinant of plasma FXIII concentration., PMID:37883802
Changes in the liver of Tinca tinca under successive domestication using an integrated multi-omics approach., PMID:37354750
Excavation of diagnostic biomarkers and construction of prognostic model for clear cell renal cell carcinoma based on urine proteomics., PMID:37260987
Identification of a novel mutation in the factor XIII A subunit in a patient with inherited factor XIII deficiency., PMID:37059930
Identification of thrombotic biomarkers in orthopedic surgery patients by plasma proteomics., PMID:36944974
Label-free serum proteomics for the identification of the putative biomarkers of postoperative pain in patients with gastric cancer., PMID:36892434
Proteomic analysis of small extracellular vesicles from the plasma of patients with hepatocellular carcinoma., PMID:36471393
Genetic landscape in coagulation factor XIII associated defects - Advances in coagulation and beyond., PMID:36372609
Blood-based protein biomarkers for the diagnosis of acute stroke: A discovery-based SWATH-MS proteomic approach., PMID:36237606
Transient Platelet Dysfunction in Congenital Factor XIII Deficiency with Enhanced Thrombin Generation Potential., PMID:35975501
Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)., PMID:35873600
[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
Targeted proteomics for evaluating risk of venous thrombosis following traumatic lower-leg injury or knee arthroscopy., PMID:34919779
Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement., PMID:31340840
Disruption of Structural Disulfides of Coagulation FXIII-B Subunit; Functional Implications for a Rare Bleeding Disorder., PMID:31013569
Inherited genetic predispositions in F13A1 and F13B genes predict abdominal adhesion formation: identification of gender prognostic indicators., PMID:30446716
Pathogenicity analysis of variations and prenatal diagnosis in a hereditary coagulation factor XIII deficiency family., PMID:29307277
Plasma protein profiling in patients undergoing coronary artery bypass grafting surgery and clinical significance., PMID:28947991
Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A2., PMID:28520207
Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII Action., PMID:27363989
Neoplasm-induced bleeding in inherited, heterozygous FXIII-A deficiency., PMID:26540128
Structural and functional influences of coagulation factor XIII subunit B heterozygous missense mutants., PMID:26247044
Assessment of Proteins Associated With Complement Activation and Inflammation in Maculae of Human Donors Homozygous Risk at Chromosome 1 CFH-to-F13B., PMID:26218915
Clinical features of 32 new Japanese cases with autoimmune haemorrha-philia due to anti-factor XIII antibodies., PMID:25929725
Factor XIII B subunit polymorphisms and the risk of coronary artery disease., PMID:25569091
Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms., PMID:24503678
In vitro secretion deficits are common among human coagulation factor XIII subunit B missense mutants: correlations with patient phenotypes and molecular models., PMID:23913518
Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth., PMID:23591632
Genetic influences on the outcome of anti-vascular endothelial growth factor treatment in neovascular age-related macular degeneration., PMID:23582991
Inclusion of genotype with fundus phenotype improves accuracy of predicting choroidal neovascularization and geographic atrophy., PMID:23523162
A common F13A1 intron 1 variant IVS1+12(A) is associated with mild FXIII deficiency in Caucasian population., PMID:23508224
Alloantibodies against the B subunit of plasma factor XIII developed in its congenital deficiency., PMID:23407795
Modulation of mouse coagulation gene transcription following acute in vivo delivery of synthetic small interfering RNAs targeting HNF4α and C/EBPα., PMID:22675511
Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration., PMID:22558131
Prothrombotic gene variants and mortality after cerebral ischemia of arterial origin., PMID:21986109
Clinical validation of a genetic model to estimate the risk of developing choroidal neovascular age-related macular degeneration., PMID:21807600
An update of the mutation profile of Factor 13 A and B genes., PMID:21640452
Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency., PMID:20331752
Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function., PMID:20179087
Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect., PMID:19937244
Factor XIII Deficiency., PMID:19598071
Natural selection and the molecular basis of electrophoretic variation at the coagulation F13B locus., PMID:18716611
For research use only. Not for human or drug use.
