Antibody data
- Antibody Data
- Antigen structure
- References [1]
- Comments [0]
- Validations
- Western blot [1]
- Immunohistochemistry [1]
- Other assay [1]
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Validation data
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- Product number
- PA5-38806 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- Anti-Phospho-PDCD4 (Ser457) Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µg
- Concentration
- 1 mg/mL
- Storage
- -20°C
Submitted references LymphoAtlas: a dynamic and integrated phosphoproteomic resource of TCR signaling in primary T cells reveals ITSN2 as a regulator of effector functions.
Locard-Paulet M, Voisinne G, Froment C, Goncalves Menoita M, Ounoughene Y, Girard L, Gregoire C, Mori D, Martinez M, Luche H, Garin J, Malissen M, Burlet-Schiltz O, Malissen B, Gonzalez de Peredo A, Roncagalli R
Molecular systems biology 2020 Jul;16(7):e9524
Molecular systems biology 2020 Jul;16(7):e9524
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of Phospho-PDCD4 pSer457 in extracts from 293 cells using a Phospho-PDCD4 pSer457 polyclonal antibody (Product # PA5-38806).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunohistochemical analysis of Phospho-PDCD4 pSer457 in paraffin-embedded human breast carcinoma using a Phospho-PDCD4 pSer457 polyclonal antibody (Product # PA5-38806).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 4 Dynamics of kinase activities Heat map showing kinase activities based on enrichment of their specific substrates for each cluster. Black dots indicate clusters with significantly enriched kinase activity (hypergeometric test P -value = 2, number of annotated sites >= 2; gray squares: fold change < 1). t-SNE plot displaying local enrichment of phosphosites corresponding to known substrates associated with the specified kinase. Dot transparency is scaled according to the P -value corresponding to the local enrichment of the annotation term (hypergeometric test, see Materials and Methods for more detailed information). Illustration of the kinase-substrate interconnections characterizing the AMPK, AKT, and ERK signaling pathways. Substrate phosphosites dynamics are displayed and color-coded according to their clusters, and the corresponding scaled kinetics are presented on the right. Immunoblot analysis of equal amounts of proteins from total lysates of CD4 + T cells treated with DMSO, U0126 (10 muM), or AKTi VIII (10 muM) and left unstimulated (-) or stimulated for 15, 120, or 300 s with anti-CD3 and anti-CD4 antibodies, probed with the indicated phospho-specific antibodies. Anti-ERK1/2 immunoblot served as a loading control. Equal amounts of proteins from total lysates of CD4 + T cells left unstimulated (-) or stimulated for 120, 300, or 600 s with anti-CD3 and anti-CD4 antibodies were analyzed by immunoblot with antibodies probing the indicated