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TXNL4A Protein (Myc-DYKDDDDK Tag)

TXNL4A 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2734686
发货至: 中国
  • 抗原 See all TXNL4A 蛋白
    TXNL4A (Thioredoxin-Like 4A (TXNL4A))
    蛋白类型
    Recombinant
    宿主
    • 3
    • 1
    资源
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This TXNL4A protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human TXNL4A / DIM1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product TXNL4A 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    TXNL4A (Thioredoxin-Like 4A (TXNL4A))
    别名
    Txnl4a,dim1 (TXNL4A 产品)
    别名
    Txnl4 Protein, TXNL4A Protein, txnl4a Protein, dim1 Protein, MGC85128 Protein, DIB1 Protein, DIM1 Protein, HsT161 Protein, SNRNP15 Protein, TXNL4 Protein, U5-15kD Protein, D18Wsu98e Protein, Dim1 Protein, ENSMUSG00000057130 Protein, U5-15kDa Protein, thioredoxin-like 4A Protein, thioredoxin like 4A Protein, thioredoxin like 4A S homeolog Protein, Txnl4a Protein, TXNL4A Protein, txnl4a Protein, LOC664328 Protein, txnl4a.S Protein
    背景
    The protein encoded by this gene is a member of the U5 small ribonucleoprotein particle (snRNP), and is involved in pre-mRNA splicing. This protein contains a thioredoxin-like fold and it is expected to interact with multiple proteins. Protein-protein interactions have been observed with the polyglutamine tract-binding protein 1 (PQBP1). Mutations in both the coding region and promoter region of this gene have been associated with Burn-McKeown syndrome, which is a rare disorder characterized by craniofacial dysmorphisms, cardiac defects, hearing loss, and bilateral choanal atresia. A pseudogene of this gene is found on chromosome 2. Alternative splicing results in multiple transcript variants.
    分子量
    16.6 kDa
    NCBI登录号
    NP_006692
    途径
    Ribonucleoprotein Complex Subunit Organization
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