PLEKHM Anticuerpos

Presentamos HOVERcruz™,

un sistema único para la rápida identificación de PLEKHM Anticuerpos. Desplace el puntero sobre los nombres de los productos de la tabla para ver los datos representativos de cada producto.

¡Chat en linea está disponible! (haga click aquí)

Nuestro sistema de chat en linea está disponible para contestar sus preguntas sobre pedidos y productos.

Vea tambiénPLEKHM Antibodies incluyendo, PLEKHM1, PLEKHM2, PLEKHM3

NOMBRE DEL PRODUCTO	NÚMERO DEL CATÁLOGO:	ISOTIPO	EPíTOPO	APLICACIONES	ESPECIES
PLEKHM1 (E-14)	sc-161158	cabra IgG	N-terminal (h)	WB, IF, ELISA	m, r, h, e, c, b, p
PLEKHM1 (P-14)	sc-161160	cabra IgG	Internal (h)	WB, IF, ELISA	m, r, h
PLEKHM2 (N-13)	sc-136808	conejo IgG	N-terminal (h)	WB, IF, ELISA	m, r, h, b, a
PLEKHM2 (C-13)	sc-136806	conejo IgG	C-terminal (h)	WB, IF, ELISA	m, r, h, e, c, b, p, a
PLEKHM3 (N-12)	sc-168976	cabra IgG	N-terminal (h)	WB, IP, IF, ELISA	m, r, h, e, c, b, a
PLEKHM3 (E-15)	sc-168974	cabra IgG	Internal (h)	WB, IF, ELISA	m, r, h, e, c, b

PLEKHM silenciadores génicos siARN, Plásmidos de shARN y Partículas Lentivirales shRNA incluyendo:

siRNAs	Plásmidos shRNA	shRNA partículas antivirales
PLEKHM1 siRNA (h): sc-93882	PLEKHM1 shRNA Plasmid (h): sc-93882-SH	PLEKHM1 shRNA (h) Partículas Lentiviral :sc-93882-V
PLEKHM1 siRNA (m): sc-152320	PLEKHM1 shRNA Plasmid (m): sc-152320-SH	PLEKHM1 shRNA (m) Partículas Lentiviral :sc-152320-V
PLEKHM2 siRNA (h): sc-88804	PLEKHM2 shRNA Plasmid (h): sc-88804-SH	PLEKHM2 shRNA (h) Partículas Lentiviral :sc-88804-V
PLEKHM2 siRNA (m): sc-152321	PLEKHM2 shRNA Plasmid (m): sc-152321-SH	PLEKHM2 shRNA (m) Partículas Lentiviral :sc-152321-V
PLEKHM3 siRNA (m): sc-152322	PLEKHM3 shRNA Plasmid (m): sc-152322-SH	PLEKHM3 shRNA (m) Partículas Lentiviral :sc-152322-V

PLEKHM1 is a 779 amino acid protein that contains two Pleckstrin homology (PH) domains, which are found in proteins that are involved in intracellular signaling. PLEKHM1 is located in the cytoplasm where it is involved in osteoclast vesicular transport and is therefore an essential protein for bone resorption. Individuals having defects in PLEKHM1 are afflicted with osteopetrosis autosomal recessive type 6 (OPTB6), a rare genetic disease that is characterized by abnormally dense bone due to ineffective bone resorption. Specifically, it is likely that mutations in the PLEKHM1 gene affect endosomal acidification/maturation and TRACP exocytosis, which has implications on osteoclast-osteoblast cross-talk. PLEKHM2 is a 1,019 amino acid cytoplasmic protein responsible for maintaining Golgi apparatus organization. Containing one PH domain and a single RUN domain, PLEKHM2 may control vacuolar membrane dynamics by regulating kinesin activity in the bacterial vacuole. PLEKHM3 is a 761 amino acid phosphoprotein that contains two PH domains and one phorbol-ester/DAG-type zinc finger.