抗体

MET2B rabbit Polyclonal Antibody

MET2B抗体
MET2B抗体应用:WB 1:500-2000This gene is a member of a family of methyltransferases that share homology with, but are distinct from, the UbiE family of methyltransferases. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008],

METH rabbit Polyclonal Antibody

METH抗体
METH抗体应用:WB 1:500-2000This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014],

MEX3B rabbit Polyclonal Antibody

MEX3B抗体
MEX3B抗体应用:WB 1:500-2000 This gene encodes an RNA-binding phosphoprotein that is part of the MEX3 (muscle excess 3) family of translational regulators. The encoded protein contains N-terminal nuclear export and nuclear localization signals and is exported from the cytoplasm to the nucleus. The protein binds to RNA via two KH domains and also colocalizes with MEX3A, Dcp1A decapping factor and Argonaute proteins within P (processing) bodies. [provided by RefSeq, Oct 2012],

MFAP5 rabbit Polyclonal Antibody

MFAP5抗体
MFAP5抗体应用:WB 1:500-2000 ELISA 1:5000-20000microfibrillar associated protein 5(MFAP5) Homo sapiens This gene encodes a 25-kD microfibril-associated glycoprotein which is a component of microfibrils of the extracellular matrix. The encoded protein promotes attachment of cells to microfibrils via alpha-V-beta-3 integrin. Deficiency of this gene in mice results in neutropenia. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014],

MFGM rabbit Polyclonal Antibody

MFGM抗体
MFGM抗体应用:WB 1:500-2000 ELISA 1:5000-20000milk fat globule-EGF factor 8 protein(MFGE8) Homo sapiens This gene encodes a preproprotein that is proteolytically processed to form multiple protein products. The major encoded protein product, lactadherin, is a membrane glycoprotein that promotes phagocytosis of apoptotic cells. This protein has also been implicated in wound healing, autoimmune disease, and cancer. Lactadherin can be further processed to form a smaller cleavage product, medin, which comprises the major protein component of aortic medial amyloid (AMA). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015],

MFN1 rabbit Polyclonal Antibody

MFN1抗体
MFN1抗体应用:WB 1:500-2000 ELISA 1:5000-20000The protein encoded by this gene is a mediator of mitochondrial fusion. This protein and mitofusin 2 are homologs of the Drosophila protein fuzzy onion (Fzo). They are mitochondrial membrane proteins that interact with each other to facilitate mitochondrial targeting. [provided by RefSeq, Jul 2008],

MFRP rabbit Polyclonal Antibody

MFRP抗体
MFRP抗体应用:WB 1:500-2000 ELISA 1:5000-20000membrane frizzled-related protein(MFRP) Homo sapiens This gene encodes a member of the frizzled-related protein family. The encoded protein plays an important role in eye development and mutations in this gene have been associated with nanophthalmos, posterior microphthalmia, retinitis pigmentosa, foveoschisis, and optic disc drusen. The protein is encoded by a bicistronic transcript which also encodes C1q and tumor necrosis factor related protein 5 (C1QTNF5). [provided by RefSeq, Jun 2013],

MFSD7 rabbit Polyclonal Antibody

MFSD7抗体
MFSD7抗体应用:WB 1:500-2000

MFSD8 rabbit Polyclonal Antibody

MFSD8抗体
MFSD8抗体应用:WB 1:500-2000 ELISA 1:5000-20000major facilitator superfamily domain containing 8(MFSD8) Homo sapiens This gene encodes a ubiquitous integral membrane protein that contains a transporter domain and a major facilitator superfamily (MFS) domain. Other members of the major facilitator superfamily transport small solutes through chemiosmotic ion gradients. The substrate transported by this protein is unknown. The protein likely localizes to lysosomal membranes. Mutations in this gene are correlated with a variant form of late infantile-onset neuronal ceroid lipofuscinoses (vLINCL). [provided by RefSeq, Oct 2008],

MGRN1 rabbit Polyclonal Antibody

MGRN1抗体
MGRN1抗体应用:WB 1:500-2000 ELISA 1:5000-20000mahogunin ring finger 1(MGRN1) Homo sapiens Mahogunin (MGRN1) is a C3HC4 RING-containing protein with E3 ubiquitin ligase activity in vitro.[supplied by OMIM, Apr 2004],
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