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POMT1 抗体 (AA 400-460)

POMT1 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2747310
发货至: 中国
  • 抗原 See all POMT1 抗体
    POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))
    抗原表位
    • 15
    • 10
    • 10
    • 7
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 400-460
    适用
    • 42
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 43
    克隆类型
    • 43
    多克隆
    标记
    • 17
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This POMT1 antibody is un-conjugated
    应用范围
    • 28
    • 18
    • 17
    • 16
    • 13
    • 13
    • 7
    • 3
    • 2
    • 1
    Western Blotting (WB), ELISA
    产品特性
    POMT1- selective antibodies were generated against a peptide taken from the N-terminal region of the human protein. The POMT1-selective antibodies are affinity purified on an immobilized antigen based affinity matrix, the isolated antibodies were then stabilized in antibody stabilization buffer for long-term storage. The anti- POMT1-selective antibodies are fully characterized for applications in western blotting and ELISA at the recommended dilutions. antibodies-online.com provides POMT1 Western blot positive control samples in SDS-PAGE sample buffer.
    纯化方法
    Affinity Purified
    免疫原
    Synthetic peptide taken within amino acid region 400-460 on human POMT1 protein.
    亚型
    IgG
    Top Product
    Discover our top product POMT1 Primary Antibody
  • 应用备注
    Antibodies were tested in ELISA and western blotting applications at 1:500 dilution using ABIN1686541 samples. Antibody dilutions for these antibodies are for reference only, investigators are expected to determine the optimal conditions.Application of this antibody in other protocols has not yet tested.
    WB: > 1:500
    IMM & IP pull-down assays: n.d.
    IHC: n.d.
    Investigators using this antibody in protocols other than listed above can request a complimentary sample of this antibody. n.d. not necessarily means the antibody is not suitable for that application, it simply means we have not yet characterized the antibody for that application.
    The antibody labels a strong band of POMT1 at 57 kDa in ABIN1686541 samples and in other cancer cell lines.
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.55-0.75 μg/μL
    储存条件
    -20 °C
    储存方法
    Storage of very dilute antibody solutions is not recommended.
  • 抗原
    POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))
    别名
    POMT1 (POMT1 产品)
    别名
    LGMD2K antibody, MDDGA1 antibody, MDDGB1 antibody, MDDGC1 antibody, RT antibody, AI505244 antibody, protein O-mannosyltransferase 1 antibody, protein-O-mannosyltransferase 1 antibody, POMT1 antibody, Pomt1 antibody
    背景
    Protein O mannosylation is initiated in the endoplasmic reticulum by protein O-mannosyl transferases (POMT proteins). They play an important role in the secretion, localization, and function of many proteins, as well as in cell wall integrity and morphogenesis in fungi. On the molecular level, the O-mannosylation pathway and the function of O-mannosyl glycans are characterized best in the eukaryotic model yeast Saccharomyces cerevisiae. O-mannosylation defects interfere with cell wall integrity and ER homeostasis in yeast, resulting in severe neuromuscular diseases in humans. Transfer of this knowledge from yeast to mammals could lead to the development of novel antifungal drugs by diagnostic and therapeutic approaches in the frame of neuromuscular diseases. The POMT family is classified into POMT1, POMT2 and POMT4 subfamilies. Protein-O-Mannosyl Transferase 1 (POMT1) is a glycosyltransferase involved in α-dystroglycan (α-DG) glycosylation. The POMT1 (protein O-mannosyl transferase 1) protein consists of 747 amino acids with seven to twelve transmembrane regions and a C-terminal ER membrane retention signal. RT-PCR reveals several mRNA splice variants. RNA dot blot analysis indicates ubiquitous expression of POMT1, with maximum levels in testis and high levels in fetal brain and pituitary tissues. Walker-Warburg syndrome (WWS), a severe, recessive, congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities, is caused by mutations in the POMT1 gene. A defect in this gene also causes limb-girdle muscular dystrophy type 2K (LGMD 2K). POMT1 is an O-mannosyl transferase that requires interaction with the product of the POMT2 gene for enzymatic function. Several transcript variants encoding different isoforms exist for this gene. In yeast, cell morphology and cell-cell separation are affected by lack of O-mannosylation resulting in abnormal cell wall and septum formation. The gene for POMT1 is present on chromosome 9q34.1
    NCBI登录号
    NP_009102
    UniProt
    Q9Y6A1
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