TNRC6B 抗体 (AA 25-70) (Biotin)
Quick Overview for TNRC6B 抗体 (AA 25-70) (Biotin) (ABIN1391569)
抗原
See all TNRC6B 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 25-70
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预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human TNRC6B
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亚型
- IgG
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anti-Trinucleotide Repeat Containing 6B (TNRC6B) (AA 153-252) antibody
TNRC6B 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 3G11 unconjugated
anti-Trinucleotide Repeat Containing 6B (TNRC6B) (AA 639-779) antibodyTNRC6B 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Trinucleotide Repeat Containing 6B (TNRC6B) (AA 253-352) antibodyTNRC6B 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4B11 unconjugated
anti-Trinucleotide Repeat Containing 6B (TNRC6B) (AA 396-445) antibodyTNRC6B 适用: 人, 小鼠, 大鼠, 豚鼠, 马, Cow, 犬, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Trinucleotide Repeat Containing 6B (TNRC6B) (AA 180-229) antibodyTNRC6B 适用: 人, 小鼠, 大鼠, 豚鼠, 马, 兔, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Trinucleotide Repeat Containing 6B (TNRC6B) (N-Term) antibodyTNRC6B 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C for 12 months.
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有效期
- 12 months
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- TNRC6B (Trinucleotide Repeat Containing 6B (TNRC6B))
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别名
- TNRC6B
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背景
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Synonyms: KIAA1093, TNRC 6B, Trinucleotide repeat containing 6B, Trinucleotide repeat containing gene 6B protein, TNR6B_HUMAN.
Background: TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
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途径
- Fc-epsilon Receptor Signaling Pathway, Regulatory RNA Pathways, EGFR Signaling Pathway
抗原
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