MKL2抗体应用：WB 1:500-2000 ELISA 1:5000-20000domain:The N-terminal region is required for nuclear localization and the C-terminal region mediates transcriptional activity.,function:Acts as a transcriptional coactivator of serum response factor (SRF). Required for skeletal myogenic differentiation.,PTM:O-glycosylated.,similarity:Contains 1 SAP domain.,similarity:Contains 3 RPEL repeats.,subunit:Interacts with MKL1 and SRF.,

MKX抗体应用：WB 1:500-2000 ELISA 1:5000-20000mohawk homeobox(MKX) Homo sapiens The protein encoded by this gene is an IRX family-related homeobox protein that may play a role in cell adhesion. Studies in mice suggest that this protein may be a regulator of tendon development. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Jun 2011],

MLEC抗体应用：WB 1:500-2000This gene encodes the carbohydrate-binding protein malectin which is a Type I membrane-anchored endoplasmic reticulum protein. This protein has an affinity for Glc2Man9GlcNAc2 (G2M9) N-glycans and is involved in regulating glycosylation in the endoplasmic reticulum. This protein has also been shown to interact with ribophorin I and may be involved in the directing the degradation of misfolded proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015],

MLF2抗体应用：WB 1:500-2000 ELISA 1:5000-20000similarity:Belongs to the MLF family.,tissue specificity:Ubiquitously expressed.,

MLL2抗体应用：IHC-p 1:50-300lysine methyltransferase 2D(KMT2D) Homo sapiens The protein encoded by this gene is a histone methyltransferase that methylates the Lys-4 position of histone H3. The encoded protein is part of a large protein complex called ASCOM, which has been shown to be a transcriptional regulator of the beta-globin and estrogen receptor genes. Mutations in this gene have been shown to be a cause of Kabuki syndrome. [provided by RefSeq, Oct 2010],

MLL4抗体应用：IHC-p 1:50-300lysine methyltransferase 2B(KMT2B) Homo sapiens This gene encodes a protein which contains multiple domains including a CXXC zinc finger, three PHD zinc fingers, two FY-rich domains, and a SET (suppressor of variegation, enhancer of zeste, and trithorax) domain. The SET domain is a conserved C-terminal domain that characterizes proteins of the MLL (mixed-lineage leukemia) family. This gene is ubiquitously expressed in adult tissues. It is also amplified in solid tumor cell lines, and may be involved in human cancer. Two alternatively spliced transcript variants encoding distinct isoforms have been reported for this gene, however, the full length nature of the shorter transcript is not known. [provided by RefSeq, Jul 2008],

MLP3C抗体应用：WB 1:500-2000 ELISA 1:5000-20000microtubule associated protein 1 light chain 3 gamma(MAP1LC3C) Homo sapiens Autophagy is a highly regulated bulk degradation process that plays an important role in cellular maintenance and development. MAP1LC3C is an ortholog of the yeast autophagosome protein Atg8 (He et al., 2003 [PubMed 12740394]).[supplied by OMIM, Nov 2010],

MLRS抗体应用：WB 1:500-2000 ELISA 1:5000-20000miscellaneous:This chain binds calcium.,similarity:Contains 3 EF-hand domains.,subunit:Myosin is an hexamer of 2 heavy chains and 4 light chains.,tissue specificity:Expressed in fetal and adult skeletal muscle.,

MMAC抗体应用：WB 1:500-2000 The exact function of the protein encoded by this gene is not known, however, its C-terminal region shows similarity to TonB, a bacterial protein involved in energy transduction for cobalamin (vitamin B12) uptake. Hence, it is postulated that this protein may have a role in the binding and intracellular trafficking of cobalamin. Mutations in this gene are associated with methylmalonic aciduria and homocystinuria type cblC. [provided by RefSeq, Oct 2009],

MMEL1抗体应用：WB 1:500-2000 ELISA 1:5000-20000membrane metalloendopeptidase like 1(MMEL1) Homo sapiens The protein encoded by this gene is a member of the neutral endopeptidase (NEP) or membrane metallo-endopeptidase (MME) family. Family members play important roles in pain perception, arterial pressure regulation, phosphate metabolism and homeostasis. This protein is a type II transmembrane protein and is thought to be expressed as a secreted protein. This gene is expressed mainly in testis with weak expression in the brain, kidney, and heart. [provided by RefSeq, Jul 2008],