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External Genitalia Morphogenesis Pathway Bioinformatics

Disease and disorder research has been conducted in relation to the External Genitalia Morphogenesis Pathway and Urethral Diseases, Nervousness, Cryptorchidism, Hypospadias, Feminization. The study of the External Genitalia Morphogenesis Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The External Genitalia Morphogenesis Pathway has been researched in relation to Genitalia Morphogenesis, Gland Morphogenesis, Mammary Gland Morphogenesis, Fertilization, Genitalia Development. The External Genitalia Morphogenesis Pathway complements our catalog of research reagents including antibodies and ELISA kits against DDR1, MME, TAC1, TFF2.

Top Research Reagents

We have 621 products for the study of the External Genitalia Morphogenesis Pathway that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

AF1126
<P align=left>Neprilysin/CD10 was detected in perfusion fixed frozen sections of mouse brain (glial cell in hippocampus) using 15 µg/mL Goat Anti-Mouse Neprilysin/CD10 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1126) overnight at 4 °C. Tissue was stained (red) and counterstained (green). View our protocol for <A class=NoLineLink href=Astrocyte‐specific Stat3 deletion increases microglial A beta  internalization and degradation, and reduces apoE expression, dystrophic neurites, and detrimental cytokinesAInternalization of A beta  (stained with IC16 antibody or methoxy‐XO4) was assessed using an engulfment assay, in which glial and A beta  structures were surface‐rendered and A beta  volumes co‐localized with glial volumes were quantified. Scale bars, 10 μm.B, CMicroglia (left Y axes) from APP/PS1 mice internalized significantly more A beta  positive for IC16 or methoxy‐XO4 when Stat3 was deleted in astrocytes (*P < 0.05, Mann–Whitney test), whereas no changes were seen in astrocytes (right axes; APP/PS1‐Stat3WT, n = 8 (four females and four males) mice; APP/PS1‐Stat3KO, n = 11 (five females and six males) mice; age, 11 months; Mann–Whitney test).D–H(D–F) Western blot quantification of protein levels of the A beta ‐degrading enzymes neprilysin/CD10 and CD36, as well as the A beta ‐binding apolipoprotein E (apoE), revealed a significantly increased expression of neprilysin and CD36 and a decreased expression of apoE (APP/PS1‐Stat3WT, n = 9 (five females and four males) mice; APP/PS1‐Stat3KO, n = 9 (five females and four males) mice; age, 11 months; *P < 0.05, Mann–Whitney test for all comparisons). (G) In contrast, TREM2 expression remained unchanged (APP/PS1‐Stat3WT, n = 8 (four females and four males) mice; APP/PS1‐Stat3KO, n = 7 (four females and three males) mice; age, 11 months; Mann–Whitney test). (H) Western blots for proteins analyzed in (D‐G).Data information: Data are represented as mean ± SEM.Source data are available online for this figure. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/30617153), licensed under a CC-BY license. Not internally tested by R&D Systems.

Goat Polyclonal
Species Mouse
Applications WB, IHC, IP

22 Publications
MAB4077
    TFF2  was detected in immersion fixed paraffin-embedded sections of human stomach  using Mouse Anti-Human TFF2 Monoclonal Antibody (Catalog # MAB4077) at  1.7 µg/mL for 1 hour at room temperature followed by  incubation with the Anti-Mouse IgG VisUCyte™  HRP Polymer Antibody (Catalog #  <a class=

Mouse Monoclonal
Species Human
Applications WB, IHC

1 Publication
AF2396
Western blot shows lysates of K562 human chronic myelogenous leukemia cell line and MCF-7 human breast cancer cell line. PVDF membrane was probed with 1 µg/mL of Goat Anti-Human DDR1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2396) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # <a class=DDR1 was detected in immersion fixed paraffin-embedded sections of human breast cancer tissue using Human DDR1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2396) at 15 µg/mL overnight at 4 °C. Before incubation with the primary antibody tissue was subjected to heat-induced epitope retrieval using Antigen Retrieval Reagent-Basic (Catalog # <a class=

Goat Polyclonal
Species Human
Applications WB, Simple Western, IHC

     1 Review

12 Publications
KGE007
N/A Substance P [Biotin]N/A Substance P [Biotin]


Species Multi-Species
Applications ELISA

37 Publications

Related Genes

The External Genitalia Morphogenesis Pathway has been researched against:

Related Pathways

The External Genitalia Morphogenesis Pathway has been linked to:

Related Diseases

The External Genitalia Morphogenesis Pathway has been studied in relation to diseases such as: