PLEKHH1 (Pleckstrin Homology, MyTH4 And FERM Domain Containing H1) is a Protein Coding gene. Diseases associated with PLEKHH1 include Gestational Trophoblastic Neoplasm. Critical component of the guidance pathway underlying endothelial cell migration and blood vessel patterning. Involved in mediating membrane localization of ephrin proteins, which have been shown to provide guidance cues for endothelial cell migration.
Background References
1. Ota T et al. Complete sequencing and characterization of 21,243 full-length human cDNAs. Nat Genet 36:40-45 (2004).
Pleckstrin homology domain containing, family H (with MyTH4 domain) member 1 antibody
pleckstrin homology domain-containing family H member 1 antibody
Images
Western blot analysis of PLEKHH1 on A431 (Human epidermoid carcinoma skin squamous cell) lysates with Mouse anti-PLEKHH1 antibody (EM1701-48) at 1/1,000 dilution.
Lysates/proteins at 20 µg/Lane. Exposure time: 1 minutes; ECL: K1801
Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: EM1701-48, 1/1,000 in primary antibody dilution buffer (K1803), overnight at 4 ℃ Secondary antibody: Goat anti-Mouse IgG-HRP (HA1006), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature
Predicted band size: 151.2 kDa Observed band size: 35 kDa
Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-PLEKHH1 antibody. Counter stained with hematoxylin.
Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-PLEKHH1 antibody. Counter stained with hematoxylin.
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