Antibody data
- Antibody Data
- Antigen structure
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- Validations
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- Product number
- PA5-79527 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- CD41 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- Reconstitute with 0.2 mL of distilled water to yield a concentration of 500 µg/mL.
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µg
- Concentration
- 500 µg/mL
- Storage
- -20°C
Submitted references Platelet-endothelial associations may promote cytomegalovirus replication in the salivary gland in mice.
Model-dependent contributions of FXII and FXI to venous thrombosis in mice.
Braxton AM, Chalmin AL, Najarro KM, Brockhurst JK, Johnson KT, Lyons CE, Daly B, Cryer CG, Vijay S, Cyphers G, Guerrero-Martin SM, Aston SA, McGee K, Su YP, Arav-Boger R, Metcalf Pate KA
Platelets 2020 Oct 2;31(7):860-868
Platelets 2020 Oct 2;31(7):860-868
Model-dependent contributions of FXII and FXI to venous thrombosis in mice.
Grover SP, Olson TM, Cooley BC, Mackman N
Journal of thrombosis and haemostasis : JTH 2020 Nov;18(11):2899-2909
Journal of thrombosis and haemostasis : JTH 2020 Nov;18(11):2899-2909
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Supportive validation
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- Invitrogen Antibodies (provider)
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- Experimental details
- 2 FIGURE Composition of thrombi formed using the mouse IVC stenosis and stasis models of thrombosis. Thrombus composition was assessed by western blotting of total soluble protein lysates from thrombi formed using the IVC stenosis and IVC stasis models of thrombosis (n = 7 per group). A, Representative western blots for fibrin(ogen), the platelet marker CD41, the neutrophil marker Ly6G, the cytoplasmic marker beta Actin, citrullinated histone H3 (H3Cit), and the nuclear marker total histone H3 (H3) in thrombi formed using the IVC stenosis and IVC stasis models. Densitometric analysis of (B) fibrin(ogen), (C) CD41, (D) Ly6G, (E) beta Actin, (F) H3Cit, and (G) H3 in thrombi formed in the IVC stenosis model compared with the IVC stasis model. H, The ratio of H3Cit to total H3 was significantly higher in thrombi formed in the IVC stenosis model compared with the IVC stasis model. * P < .05, ** P < .01 Mann-Whitney U test. Data represented as individual values with a line for the median
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- Invitrogen Antibodies (provider)
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- Experimental details
- 3 FIGURE Composition of thrombi formed using the IVC stasis is F12 +/+ mice compared with F12 -/- mice and F11 +/+ mice compared with F11 -/- mice. Thrombus composition was assessed in thrombi from F12 -/- and F11 -/- mice formed using the IVC stasis model of thrombosis by western blotting of total soluble protein lysates and compared with respective wild-type littermate controls. Densitometric analysis of immunoblots for (A, H) fibrin(ogen), (B, I) CD41, (C, J) Ly6G, (D, K) beta actin, (E, L) citrullinated histone H3, and (F, M) total histone H3 for F12 -/- , F11 -/- mice and wild-type littermate controls. (G, N) The ratio of H3Cit to total H3 was also calculated. * P < .01 Mann-Whitney U test. Data represented as individual values plus the median
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- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 3. Sequestration of platelets in PEAs corresponds with platelet decline during acute mCMV infection. (A) Representative immunohistochemistry images (400x) of CD41+ platelets (brown, indicated by black arrowhead) bound to CD34+ vessels (red) in the salivary gland of a mCMV-infected mouse. (B) Quantification of PEA formation in the salivary gland longitudinally throughout acute mCMV infection. Kruskal-Wallis analyses with Dunn's posttest, excluding outlier as determined by Grubs outlier test, bars indicate median values.