RFTN2 抗体 (AA 1-100) (AbBy Fluor® 647)
Quick Overview for RFTN2 抗体 (AA 1-100) (AbBy Fluor® 647) (ABIN1399404)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 1-100
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预测反应
- Human,Mouse,Rat,Dog,Sheep,Horse,Rabbit
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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 RFTN2
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亚型
- IgG
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anti-Raftlin Family Member 2 (RFTN2) (AA 1-300) antibody
RFTN2 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Raftlin Family Member 2 (RFTN2) (C-Term) antibodyRFTN2 适用: 人, 小鼠, 大鼠 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Raftlin Family Member 2 (RFTN2) (N-Term) antibodyRFTN2 适用: 人, Cow, 犬, 豚鼠, 马, Pig, 兔, 小鸡, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Raftlin Family Member 2 (RFTN2) (N-Term) antibodyRFTN2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- RFTN2 (Raftlin Family Member 2 (RFTN2))
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别名
- RFTN2
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背景
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Synonyms: Raft-linking protein 2, Raftlin-2, Rftn2, RFTN2_HUMAN.
Background: Membrane microdomains known as lipid rafts are implicated in B-cell activation during B-cell receptor (BCR) signal initiation. Raftlin-2, also designated RFTN2 (raftlin family member 2) or raft-linking protein 2, is a 501 amino acid cell membrane protein that is essential for raft cell assembly and maintenance. A lipid anchor protein, Raftlin-2 belongs to the raftlin family and is encoded by a gene that maps to human chromosome 2q33.1 and mouse chromosome 1 C1.2. Human chromosome 2 is the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene.
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基因ID
- 130132
抗原
-
