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- 抗原 See all TXNL4A 抗体
- TXNL4A (Thioredoxin-Like 4A (TXNL4A))
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适用
- 人, 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This TXNL4A antibody is un-conjugated
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应用范围
- 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
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anti-Thioredoxin-Like 4A (TXNL4A) (AA 1-142) antibody
TXNL4A 适用: 人 ELISA, WB 宿主: 小鼠 Monoclonal 1C4 unconjugated
anti-Thioredoxin-Like 4A (TXNL4A) (AA 1-142) antibodyTXNL4A 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Thioredoxin-Like 4A (TXNL4A) antibodyTXNL4A 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Thioredoxin-Like 4A (TXNL4A) (AA 1-142) antibodyTXNL4A 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500 - 1:2000
- 限制
- 仅限研究用
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- 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.
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- 抗原
- TXNL4A (Thioredoxin-Like 4A (TXNL4A))
- 别名
- TXNL4A (TXNL4A 产品)
- 背景
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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
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Observed_MW: 13kDa
Calculated_MW: 16kDa
- 基因ID
- 10907
- UniProt
- P83876
- 途径
- Ribonucleoprotein Complex Subunit Organization
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