MTCH2抗体应用：WB 1:500-2000 This gene encodes a member of the SLC25 family of nuclear-encoded transporters that are localized in the inner mitochondrial membrane. Members of this superfamily are involved in many metabolic pathways and cell functions. Genome-wide association studies in human have identified single-nucleotide polymorphisms in several loci associated with obesity. This gene is one such locus, which is highly expressed in white adipose tissue and adipocytes, and thought to play a regulatory role in adipocyte differentiation and biology. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A recent study showed this gene to be an authentic stop codon readthrough target, and that its mRNA can give rise to an additional C-terminally extended isoform by use of an alternative in-frame translation termination codon. [provided by RefSeq, Nov 2015],

MTF1抗体应用：WB 1:500-2000 ELISA 1:5000-20000metal regulatory transcription factor 1(MTF1) Homo sapiens This gene encodes a transcription factor that induces expression of metallothioneins and other genes involved in metal homeostasis in response to heavy metals such as cadmium, zinc, copper, and silver. The protein is a nucleocytoplasmic shuttling protein that accumulates in the nucleus upon heavy metal exposure and binds to promoters containing a metal-responsive element (MRE). [provided by RefSeq, Jul 2008],

MTFR1抗体应用：WB 1:500-2000 ELISA 1:5000-20000mitochondrial fission regulator 1(MTFR1) Homo sapiens This gene encodes a mitochondrial protein that is characterized by a poly-proline rich region. A chicken homolog of this protein promotes mitochondrial fission and the mouse homolog protects cells from oxidative stress. A related pseudogene of this gene is found on chromosome X. [provided by RefSeq, Mar 2009],

MTMR5抗体应用：WB 1:500-2000This gene encodes a member of the protein-tyrosine phosphatase family. However, the encoded protein does not appear to be a catalytically active phosphatase because it lacks several amino acids in the catalytic pocket. This protein contains a Guanine nucleotide exchange factor (GEF) domain which is necessary for its role in growth and differentiation. Mutations in this gene have been associated with Charcot-Marie-Tooth disease 4B3. Pseudogenes of this gene have been defined on chromosomes 1 and 8. [provided by RefSeq, Dec 2014],

MTNB抗体应用：WB 1:500-2000 APIP is an APAF1 (MIM 602233)-interacting protein that acts as a negative regulator of ischemic/hypoxic injury (Cho et al., 2004 [PubMed 15262985]).[supplied by OMIM, Dec 2008],

MTPN抗体应用：WB 1:500-2000 ELISA 1:5000-20000myotrophin(MTPN) Homo sapiens The transcript produced from this gene is bi-cistronic and can encode both myotrophin and leucine zipper protein 6. The myotrophin protein is associated with cardiac hypertrophy, where it is involved in the conversion of NFkappa B p50-p65 heterodimers to p50-p50 and p65-p65 homodimers. This protein also has a potential function in cerebellar morphogenesis, and it may be involved in the differentiation of cerebellar neurons, particularly of granule cells. A cryptic ORF at the 3' end of this transcript uses a novel internal ribosome entry site and a non-AUG translation initiation codon to produce leucine zipper protein 6, a 6.4 kDa tumor antigen that is associated with myeloproliferative disease. [provided by RefSeq, Jul 2008],

MTSS1抗体应用：WB 1:500-2000 ELISA 1:5000-20000domain:The WH2 motif at the C-terminus binds to actin monomers.,function:May be related to cancer progression or tumor metastasis in a variety of organ sites, most likely through an interaction with the actin cytoskeleton.,similarity:Belongs to the MTSS1 family.,similarity:Contains 1 IMD (IRSp53/MIM homology) domain.,similarity:Contains 1 WH2 domain.,subunit:Binds to actin. Binds to the cytoplasmic domain of receptor protein tyrosine phosphatase delta.,tissue specificity:Expressed in many tissues, including spleen, thymus, prostate, testis, uterus, colon, and peripheral blood.,

MTU1抗体应用：WB 1:500-2000 ELISA 1:5000-20000This nuclear gene encodes a mitochondrial tRNA-modifying enzyme. The encoded protein catalyzes the 2-thiolation of uridine on the wobble positions of tRNA(Lys), tRNA(Glu), and tRNA(Gln), resulting in the formation of 5-taurinomethyl-2-thiouridine moieties. Mutations in this gene may cause transient infantile liver failure. Polymorphisms in this gene may also influence the severity of deafness caused by mitochondrial 12S ribosomal RNA mutations. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013],

MUC15抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:May play a role in the cell adhesion to the extracellular matrix.,PTM:Highly glycosylated (N- and O-linked carbohydrates).,sequence caution:Translated as stop.,tissue specificity:Expressed in spleen, thymus, prostate, testis, ovary, small intestine, colon, peripheral blood leukocyte, bone marrow, lymph node and lung.,

MUC21抗体应用：WB 1:500-2000