WB result of Factor XIIIa Rabbit mAb
Primary antibody: Factor XIIIa Rabbit mAb at 1/1000 dilution
Lane 1: Human plasma lysate 5 µg
Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 68 kDa
Observed MW: 84 kDa
Product Details
Product Details
Product Specification
Host | Rabbit |
Antigen | Factor XIIIa |
Synonyms | Coagulation factor XIII A chain, Coagulation factor XIIIa, Protein-glutamine gamma-glutamyltransferase A chain, Transglutaminase A chain, F13A1, F13A, FXIIIA |
Immunogen | Synthetic Peptide |
Location | Cytoplasm, Secreted |
Accession | P00488 |
Clone Number | SDT-644-7 |
Antibody Type | Recombinant mAb |
Isotype | IgG |
Application | WB, IHC-P, IP |
Reactivity | Hu |
Purification | Protein A |
Concentration | 0.5 mg/ml |
Conjugation | Unconjugated |
Physical Appearance | Liquid |
Storage Buffer | PBS, 40% Glycerol, 0.05%BSA, 0.03% Proclin 300 |
Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
application | dilution | species |
WB | 1:1000 | |
IHC | 1:1000 | |
IP | 1:50 |
Background
Factor XIII is a betaglobulin found in plasma and is composed of two subunits. Factor XIIIA is the catalytic subunit. Factor XIIIa is expressed in platelets, megakaryocytes, fibroblast-like cells in the placenta, uterus, and prostate, monocytes and macrophages and dermal dendritic cells. It is most commonly recognized as a marker of fibrohistiocytic proliferations. Factor XIIIa has also been used with CD34 to differentiate between dermatofibroma and dermatofibrosarcoma protuberans.
Picture
Picture
Western Blot
IP

Factor XIIIa Rabbit mAb at 1/50 dilution (1 µg) immunoprecipitating Factor XIIIa in 0.4 mg human plasma lysate.
Western blot was performed on the immunoprecipitate using Factor XIIIa Rabbit mAb at 1/1000 dilution.
Secondary antibody (HRP) for IP was used at 1/400 dilution.
Lane 1: human plasma lysate 20 µg (Input)
Lane 2: Factor XIIIa Rabbit mAb IP in human plasma lysate
Lane 3: Rabbit monoclonal IgG IP in human plasma lysate
Predicted MW: 68 kDa
Observed MW: 84 kDa
Immunohistochemistry
IHC shows positive staining in paraffin-embedded human tonsil. Anti-Factor XIIIa antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human spleen. Anti-Factor XIIIa antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human placenta. Anti-Factor XIIIa antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human breast cancer. Anti-Factor XIIIa antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human fibrous histiocytoma. Anti-Factor XIIIa antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human dermatofibrosarcoma protuberans. Anti-Factor XIIIa antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
