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Inner nuclear membrane protein

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Below are the list of possible Inner nuclear membrane protein products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Inner nuclear membrane protein HEH2

 Inner nuclear membrane protein HEH2 ELISA Kit
 Inner nuclear membrane protein HEH2 Recombinant
 Inner nuclear membrane protein HEH2 Antibody
Also known as Inner nuclear membrane protein HEH2 (Helix-extension-helix domain-containing protein 2).
 HEH2 ELISA Kit
 HEH2 Recombinant
 HEH2 Antibody
 YDR458C ELISA Kit
 YDR458C Recombinant
 YDR458C Antibody
 D8035.2 ELISA Kit
 D8035.2 Recombinant
 D8035.2 Antibody
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Inner nuclear membrane protein Man1

 Inner nuclear membrane protein Man1 ELISA Kit
 Inner nuclear membrane protein Man1 Recombinant
 Inner nuclear membrane protein Man1 Antibody
Also known as Inner nuclear membrane protein Man1 (LEM domain-containing protein 3).
MAN1: Can function as a specific repressor of TGF-beta, activin, and BMP signaling through its interaction with the R-SMAD proteins. Antagonizes TGF-beta-induced cell proliferation arrest. Defects in LEMD3 are the cause of Buschke-Ollendorff syndrome (BOS); also known as dermatoosteopoikilosis or disseminated d
>>>
ermatofibrosis with osteopoikilosis or dermatofibrosis lenticularis disseminata with osteopoikilosis or osteopathia condensans disseminata. BOS refers to the association of osteopoikilosis with disseminated connective-tissue nevi. Osteopoikilosis is a skeletal dysplasia characterized by a symmetric but unequal distribution of multiple hyperostotic areas in different parts of the skeleton. Both elastic-type nevi (juvenile elastoma) and collagen-type nevi (dermatofibrosis lenticularis disseminata) have been described in BOS. Skin or bony lesions can be absent in some family members, whereas other relatives may have both. Defects in LEMD3 are a cause of melorheostosis (MEL). Melorheostosis is a rare mesenchymal dysplasia and one of the sclerosing bone disorders. It is caused by a developmental error, with a sclerotomal distribution, frequently involving one limb. It may be asymptomatic, but pain, stiffness with limitation of motion, leg-length discrepancy and limb deformity may occur.

Protein type: Membrane protein, integral; Membrane protein, multi-pass; Nuclear envelope

Cellular Component: integral to membrane; integral to nuclear inner membrane; nuclear envelope; nuclear inner membrane

Molecular Function: chromatin DNA binding

Biological Process: angiogenesis; blood vessel endothelial cell migration during intussusceptive angiogenesis; negative regulation of activin receptor signaling pathway; negative regulation of BMP signaling pathway; negative regulation of transforming growth factor beta receptor signaling pathway; nuclear membrane organization and biogenesis; nuclear organization and biogenesis; regulation of cell cycle
 Lemd3 ELISA Kit
 Lemd3 Recombinant
 Lemd3 Antibody
 Man1 ELISA Kit
 Man1 Recombinant
 Man1 Antibody
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Inner nuclear membrane protein SRC1

 Inner nuclear membrane protein SRC1 ELISA Kit
 Inner nuclear membrane protein SRC1 Recombinant
 Inner nuclear membrane protein SRC1 Antibody
Also known as Inner nuclear membrane protein SRC1 (Helix-extension-helix domain-containing protein 1).
Plays a role in sister chromatid separation.
 SRC1 ELISA Kit
 SRC1 Recombinant
 SRC1 Antibody
 HEH1 ELISA Kit
 HEH1 Recombinant
 HEH1 Antibody
 YML034W ELISA Kit
 YML034W Recombinant
 YML034W Antibody
 YML033W ELISA Kit
 YML033W Recombinant
 YML033W Antibody
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