Product Name
Coagulation Factor XIII B Polypeptide (F XIII B), ELISA Kit
Full Product Name
Mouse Coagulation Factor XIII B Polypeptide ELISA Kit
Product Synonym Names
F XIII B
Product Gene Name
F XIII B elisa kit
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Sample Manual Insert
Download Sample PDF Manual View Sample PDF Manual
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Samples
Serum, plasma and other
biological fluids.
Assay Type
Sandwich ELISA, Double
Antibody
Detection Range
3.125-200ng/ml
Preparation and Storage
Store at 4 degree C if kit is to be used within 1 week. Stable for 6 months (if micro ELISA Plate, Lyophilized Standard and Concentrated Biotinylated Detection Protein stored at-20 degree C. Other components at 2-8 degree C). Stable for 12 months (if the entire kit is stored at-20 degree C).
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of F XIII B elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms for F XIII B purchase
MBS762832 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Coagulation Factor XIII B Polypeptide (F XIII B) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing F XIII B. The ELISA analytical biochemical technique of the MBS762832 kit is based on F XIII B antibody-F XIII B antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect F XIII B antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, F XIII B. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
Related Product Information for
F XIII B elisa kit
Principle of the Assay||This kit was based on sandwich enzyme-linked immune-sorbent assay technology. anti-Mouse F XIII B antibody was pre-coated onto 96-well plates. And the biotin conjugated anti-Mouse F XIII B antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and wash with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the Mouse F XIII B amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of Mouse F XIII B can be calculated.
Typical Testing Data of F XIII B elisa kit
Typical Standard Curve of F XIII B elisa kit
NCBI/Uniprot data below describe general gene information for F XIII B. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001985.2
[Other Products]
NCBI GenBank Nucleotide #
NM_001994.2
[Other Products]
UniProt Secondary Accession #
Q5VYL5; A8K3E5[Other Products]
UniProt Related Accession #
P05160[Other Products]
Molecular Weight
75,511 Da
NCBI Official Full Name
coagulation factor XIII B chain
NCBI Official Synonym Full Names
coagulation factor XIII B chain
NCBI Official Symbol
F13B??[Similar Products]
NCBI Official Synonym Symbols
FXIIIB
??[Similar Products]
NCBI Protein Information
coagulation factor XIII B chain
UniProt Protein Name
Coagulation factor XIII B chain
UniProt Synonym Protein Names
Fibrin-stabilizing factor B subunit; Protein-glutamine gamma-glutamyltransferase B chain; Transglutaminase B chain
UniProt Gene Name
F13B??[Similar Products]
UniProt Entry Name
F13B_HUMAN
NCBI Summary for F XIII B
This gene encodes coagulation factor XIII B subunit. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as a plasma carrier molecules. Platelet factor XIII is comprised only of 2 A subunits, which are identical to those of plasma origin. Upon activation by the cleavage of the activation peptide by thrombin and in the presence of calcium ion, the plasma factor XIII dissociates its B subunits and yields the same active enzyme, factor XIIIa, as platelet factor XIII. This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion. [provided by RefSeq, Jul 2008]
UniProt Comments for F XIII B
F13B: The B chain of factor XIII is not catalytically active, but is thought to stabilize the A subunits and regulate the rate of transglutaminase formation by thrombin. Defects in F13B are the cause of factor XIII subunit B deficiency (FA13BD). FA13BD is an autosomal recessive disorder characterized by a life-long bleeding tendency, impaired wound healing and spontaneous abortion in affected women.
Protein type: Secreted, signal peptide; Secreted
Chromosomal Location of Human Ortholog: 1q31-q32.1
Cellular Component: extracellular region
Biological Process: blood coagulation
Disease: Factor Xiii, B Subunit, Deficiency Of
Research Articles on F XIII B
1. Genetic markers associated with low FXIIIB levels increase risk of ischemic stroke cardioembolic subtype.
Precautions
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Disclaimer
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