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TXNL4A 抗体

TXNL4A 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6566788
发货至: 中国
  • 抗原 See all TXNL4A 抗体
    TXNL4A (Thioredoxin-Like 4A (TXNL4A))
    适用
    • 8
    • 1
    • 1
    人, 小鼠
    宿主
    • 7
    • 1
    克隆类型
    • 7
    • 1
    多克隆
    标记
    • 4
    • 2
    • 1
    • 1
    This TXNL4A antibody is un-conjugated
    应用范围
    • 5
    • 3
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human TXNL4A
    亚型
    IgG
    Top Product
    Discover our top product TXNL4A Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    限制
    仅限研究用
  • 浓度
    1 mg/mL
    缓冲液
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    TXNL4A (Thioredoxin-Like 4A (TXNL4A))
    别名
    TXNL4A (TXNL4A 产品)
    别名
    Txnl4 antibody, TXNL4A antibody, txnl4a antibody, dim1 antibody, MGC85128 antibody, DIB1 antibody, DIM1 antibody, HsT161 antibody, SNRNP15 antibody, TXNL4 antibody, U5-15kD antibody, D18Wsu98e antibody, Dim1 antibody, ENSMUSG00000057130 antibody, U5-15kDa antibody, thioredoxin-like 4A antibody, thioredoxin like 4A antibody, thioredoxin like 4A S homeolog antibody, Txnl4a antibody, TXNL4A antibody, txnl4a antibody, LOC664328 antibody, txnl4a.S antibody
    背景

    Synonyms: BMKS,DIB 1,DIB1,DIM 1,DIM1,DIM1 protein homolog,HsT161,SNRNP15,Spliceosomal U5 snRNP specific 15 kDa protein,Spliceosomal U5 snRNP-specific 15 kDa protein,Thioredoxin like 4,Thioredoxin like 4A,Thioredoxin like protein 4A,Thioredoxin like U5 snRNP protein U5 15kD,Thioredoxin-like protein 4A,Thioredoxin-like U5 snRNP protein U5-15kD,TXN4A,TXNL 4,TXNL 4A,TXNL4,txnl4a,U5 15kD

    Background: 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

    Observed_MW: 13kDa

    Calculated_MW: 16kDa

    基因ID
    10907
    UniProt
    P83876
    途径
    Ribonucleoprotein Complex Subunit Organization
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