Anti-Factor XIIIa antibody [AC-1A1] (ab1834)
Key features and details
- Mouse monoclonal [AC-1A1] to Factor XIIIa
- Suitable for: IHC-P, WB, Flow Cyt
- Reacts with: Human
- Isotype: IgG1
Overview
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Product name
Anti-Factor XIIIa antibody [AC-1A1]
See all Factor XIIIa primary antibodies -
Description
Mouse monoclonal [AC-1A1] to Factor XIIIa -
Host species
Mouse -
Tested applications
Suitable for: IHC-P, WB, Flow Cytmore details -
Species reactivity
Reacts with: Human -
Immunogen
BALB/C mice were injected with recombinant human protein corresponding to A-subunit of coagulation Factor XIII.
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Positive control
- Placenta
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General notes
This antibody recognizes both the dimer and monomer forms.
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Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle. -
Storage buffer
Preservative: 0.05% Sodium azide
Constituent: 1% BSA -
Concentration information loading...
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Purity
IgG fraction -
Clonality
Monoclonal -
Clone number
AC-1A1 -
Isotype
IgG1 -
Light chain type
kappa -
Research areas
Images
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ab1834 - immunohistochemistry
Formalin fixed paraffin embedded human placenta stained with Factor XIIIa, using ABC and AEC chromogen.
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ab1834 staining human placenta by IHC-P.
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Anti-Factor XIIIa antibody [AC-1A1] (ab1834) at 1/250 dilution + Human placenta tissue lysate - total protein at 10 µg
Secondary
Goat Anti-Mouse IgG H&L (HRP) preadsorbed (ab97040) at 1/5000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 83 kDa
Observed band size: 83 kDa
Additional bands at: 37 kDa, 74 kDa. We are unsure as to the identity of these extra bands.
Exposure time: 2 minutes
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Immunohistochemical analysis of formalin-fixed, paraffin-embedded Human placenta tissue, staining Factor XIIIa with ab1834.
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Overlay histogram showing A549 cells stained with ab16956 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab16956, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.