Factor XIIIa Antibody (YA5726)

(Synonyms: Coagulation factor XIII A chain; Coagulation factor XIIIa; Protein-glutamine gamma-glutamyltransferase A chain; Transglutaminase A chain; )

Factor XIIIa Antibody (YA5726) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to Factor XIIIa.

For research use only. We do not sell to patients.
  • Host:

    Mouse

  • Isotype:

    IgG

  • Application:

    IHC-P, ELISA

  • Reactivity :

    Human, Mouse, Rat

  • Formulation:

    Supplied in PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA

  • Conjugation:
    Non-conjugated

Applications

Application
IHC-P Info
IHC-P: Immunohistochemistry-Paraffin
ELISA Info
ELISA: Enzyme Linked Immunosorbent Assay
Dilution Ratio 1:200-400 1:500-5000

Product Details

Description

Factor XIIIa Antibody (YA5726) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to Factor XIIIa.

  • Host Mouse
  • Clonality Monoclonal
  • Species Reactivity
    Human, Mouse, Rat
  • Observed Molecular Weight
    Observed band size: 83 kDa Info
    Note: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
  • Calculated Molecular Weight Predicted band size: 76 kDa,83 kDa
Immunogen

Synthesized peptide derived from human Factor XIIIa AA range: 400-500

Purification

affinity chromatography.

Conjugation

Non-conjugated

Modification

Unmodified

Isotype

IgG

Product Properties

  • Appearance

    Solution

  • Formulation

    Supplied in PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA

  • Storage & Stability

    Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.

  • Shipping

    Shipping with blue ice.

Background

  • Function

    Factor XIIIA (FXIII-A) is the catalytic subunit of coagulation factor XIII and acts as a transglutaminase that forms ε- (γ-glutamyl) lysyl cross-links in protein substrates[1]. In plasma, FXIII circulates as FXIII-A2B2, where A subunits provide catalytic activity and B subunits act as non-enzymatic carrier subunits[2]. Mechanistically, thrombin and Ca2+ convert plasma FXIII into active FXIIIa, which stabilizes fibrin clots, links α2-antiplasmin to fibrin, and protects clots from fibrinolysis[1][3]. Beyond hemostasis, FXIII-A supports wound healing, tissue repair, pregnancy maintenance, and angiogenesis, making it relevant for coagulation biology and regenerative research[1][2]. In disease models, FXIII deficiency impaired wound healing and aggravated cardiac rupture after myocardial infarction in mice[4]. In inflammatory disease, macrophage-derived FXIII-A linked extravascular coagulation to COPD-associated inflammation, while macrophage-derived foam cells expressed cellular FXIII-A in atherosclerosis-related models[5][6]. Compared with FXIII-B, FXIII-A is the enzymatic isoform and therefore provides the primary experimental target for activity assays, genetic models, and inhibitor studies[2][3]. For experimental applications, tridegin inhibits plasma and platelet FXIIIa, and structure-function studies support its use as a peptide scaffold for FXIIIa inhibitor design[7][8].

  • Subcellular Localization

    Cytoplasm; Secreted

  • Subunit

    Tetramer of two A chains (F13A1) and two B (F13B) chains

  • SwissProt ID

    P00488

  • Gene ID
  • Synonyms

    Coagulation factor XIII A chain; Coagulation factor XIIIa; Protein-glutamine gamma-glutamyltransferase A chain; Transglutaminase A chain;

References

Factor XIIIa Antibody (YA5726) Related Classifications

MOQ
Minimum order quantity
100 mg

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