MAGBA抗体应用：WB 1:500-2000 ELISA 1:5000-20000MAGE family member B10(MAGEB10) Homo sapiens This gene encodes a member of the B subfamily of the melanoma associated antigen protein family. The encoded protein is specifically expressed in testis and tumor cells. [provided by RefSeq, Apr 2010],

MAGBI抗体应用：WB 1:500-2000 ELISA 1:5000-20000similarity:Contains 1 MAGE domain.,

MAGC1抗体应用：WB 1:500-2000 ELISA 1:5000-20000MAGE family member C1(MAGEC1) Homo sapiens This gene is a member of the melanoma antigen gene (MAGE) family. The proteins of this family are tumor-specific antigens that can be recognized by autologous cytolytic T lymphocytes. This protein contains a large number of unique short repetitive sequences in front of the MAGE-homologous sequence, and therefore is about 800 aa longer than the other MAGE proteins. [provided by RefSeq, Jul 2008],

MAGC3抗体应用：WB 1:500-2000 ELISA 1:5000-20000MAGE family member C3(MAGEC3) Homo sapiens This gene is a member of the MAGEC gene family. The members of this family are not expressed in normal tissues, except for testis, and are expressed in tumors of various histological types. The MAGEC genes are clustered on chromosome Xq26-q27. Two transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008],

MAGD1抗体应用：WB 1:500-2000 ELISA 1:5000-20000MAGE family member D1(MAGED1) Homo sapiens This gene is a member of the melanoma antigen gene (MAGE) family. Most of the genes of this family encode tumor specific antigens that are not expressed in normal adult tissues except testis. Although the protein encoded by this gene shares strong homology with members of the MAGE family, it is expressed in almost all normal adult tissues. This gene has been demonstrated to be involved in the p75 neurotrophin receptor mediated programmed cell death pathway. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],

MAGD2抗体应用：WB 1:500-2000 ELISA 1:5000-20000MAGE family member D2(MAGED2) Homo sapiens This gene is a member of the MAGED gene family. The MAGED genes are clustered on chromosome Xp11. This gene is located in Xp11.2, a hot spot for X-linked mental retardation (XLMR). This gene may also be involved in several types of cancer, including breast cancer and melanoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013],

MAGD4抗体应用：WB 1:500-2000 ELISA 1:5000-20000MAGE family member D4B(MAGED4B) Homo sapiens This gene is a member of the MAGED gene family. It is expressed only in brain and ovary, and some transcript variants of this gene are specifically expressed in glioma cells. This gene is clustered with other MAGED genes on chromosome Xp11. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2011],

MAGE1抗体应用：WB 1:500-2000 ELISA 1:5000-20000MAGE family member E1(MAGEE1) Homo sapiens This gene encodes an alpha-dystrobrevin-associated MAGE (melanoma-associated antigen) protein, which is a member of the MAGE family. The protein contains a nuclear localization signal in the N-terminus, 30 12-amino acid repeats beginning at nt 60 with the consensus sequence ASEGPSTSVLPT, and two MAGE domains in the C-terminus. It may play a signaling role in brain, muscle, and peripheral nerve. This gene is located on X chromosome in a region containing loci linked to mental retardation. [provided by RefSeq, Mar 2010],

MAGE2抗体应用：WB 1:500-2000 ELISA 1:5000-20000MAGE family member E2(MAGEE2) Homo sapiens This gene encodes a member of the E subfamily of MAGE (melanoma antigen-encoding gene) gene family. The gene is intronless and the encoded protein has two of the MAGE domains which are characteristic of MAGE family proteins. [provided by RefSeq, Sep 2011],

MAGF1抗体应用：WB 1:500-2000 ELISA 1:5000-20000MAGE family member F1(MAGEF1) Homo sapiens This intronless gene encodes a member of the MAGE superfamily. It is ubiquitously expressed in normal tissues and in tumor cells. This gene includes a microsatellite repeat in the coding region. [provided by RefSeq, Jul 2008],