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The CTX (see VSIG2, MIM 606011) family of proteins, including ASAM, are type I transmembrane proteins within the Ig superfamily that localize to junctional complexes between endothelial and epithelial cells and may play a role in cell-cell adhesion (Raschperger et al., 2004 [PubMed 14573622]).[supplied by OMIM, Mar 2008].. Additionally we are shipping CLMP Antibodies (63) and CLMP Kits (8) and many more products for this protein.
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Human CLMP Protein expressed in Human Cells - ABIN2003394
Raschperger, Engstrom, Pettersson, Fuxe: CLMP, a novel member of the CTX family and a new component of epithelial tight junctions. in The Journal of biological chemistry 2003
Show all 2 references for 2003394
Rat (Rattus) CLMP Protein expressed in Human Cells - ABIN2009324
Eguchi, Wada, Hida, Zhang, Matsuoka, Baba, Hashimoto, Shikata, Ogawa, Makino: Identification of adipocyte adhesion molecule (ACAM), a novel CTX gene family, implicated in adipocyte maturation and development of obesity. in The Biochemical journal 2005
Show all 2 references for 2009324
Inhibition of CFTR (show CFTR Proteins) or histone deacetylase (HDAC (show HDAC1 Proteins)) enhanced CAR expression while CFTR (show CFTR Proteins) overexpression or restoration of the diminished HDAC (show HDAC3 Proteins) activity in cystic fibrosis (show S100A8 Proteins) cells reduced CAR expression.
Novel inherited variants in CLMP were identified in three congenital short bowel syndrome patients derived from two unrelated families.
The key processes involved in intestinal epithelial development appear to be unaffected by wild type-CLMP or mutant-CLMP.
Coxsackievirus and adenovirus receptor (show CXADR Proteins) gene expression is induced in esophageal cancer cells by the HDAC (show HDAC3 Proteins) inhibitor trichostatin A.
The PDZ1 and PDZ3 domains of MAGI-1 (show MAGI1 Proteins) regulate the eight-exon isoform of the CXADR-like membrane protein.
Loss-of-function mutations in CLMP cause congenital short bowel syndrome in human beings, likely by interfering with tight-junction formation, which disrupts intestinal development.
CLMP is a novel cell-cell adhesion molecule (show PCDHB16 Proteins) and a new component of epithelial tight junctions.
We identified ACAM (adipocyte adhesion molecule), a novel homologue of the CTX (cortical thymocyte marker (show VSIG1 Proteins) in Xenopus) gene family, which may be the critical adhesion molecule (show NCAM1 Proteins) in adipocyte differentiation and development of obesity.
ASAM, IGSF11 (show IGSF11 Proteins), CXADR (show CXADR Proteins) and ESAM (show ESAM Proteins) are type I transmembrane proteins and members of the same IGSF superfamily.
Data (including data from studies in transgenic mice) suggest that, when Acam/Clmp is abundantly expressed on plasma membrane of mature adipocytes, mice are protected from obesity and diabetes with prominent reduction of adipose tissue mass and smaller size of adipocytes; studies used high-fat, high-sucrose diet to induce obesity and diabetes in control mice.
Expression of CLMP, a novel tight junction protein (show OCLN Proteins), is mediated via the interaction of GATA (show QRSL1 Proteins) with the Kruppel family proteins, KLF4 (show KLF4 Proteins) and Sp1 (show SP1 Proteins), in mouse TM4 (show TPM4 Proteins) Sertoli cells.
TNFalpha (show TNF Proteins)-mediated mRNA degradation of the CLMP gene is controlled by TTP (show ZFP36 Proteins) through the JNK (show MAPK8 Proteins) signalling cascade
The CTX (see VSIG2, MIM 606011) family of proteins, including ASAM, are type I transmembrane proteins within the Ig superfamily that localize to junctional complexes between endothelial and epithelial cells and may play a role in cell-cell adhesion (Raschperger et al., 2004
CAR-like membrane protein
, adipocyte adhesion molecule
, adipocyte-specific adhesion molecule
, coxsackie- and adenovirus receptor-like membrane protein
, visceral adipose tissue-specific transmembrane protein OL-16
, adipocyte-specific protein 5