RBMX2 抗体 (AA 21-100) (FITC)
Quick Overview for RBMX2 抗体 (AA 21-100) (FITC) (ABIN1710658)
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 21-100
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预测反应
- Human,Mouse,Rat,Cow,Sheep,Pig,Horse,Chicken,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 RBMX2
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亚型
- IgG
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anti-RNA Binding Motif Protein, X-Linked 2 (RBMX2) (AA 242-271), (C-Term) antibody
RBMX2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB28673 unconjugated
anti-RNA Binding Motif Protein, X-Linked 2 (RBMX2) (AA 245-265), (C-Term) antibodyRBMX2 适用: 人 WB, IHC (p), EIA 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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- RBMX2 (RNA Binding Motif Protein, X-Linked 2 (RBMX2))
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别名
- RBMX2
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背景
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Synonyms: RNA-binding mot protein, X-linked 2, CGI-79, CGI 79, Rbmx2, RBMX2_HUMAN, RNA binding mot protein X linked 2, RNA-binding mot protein, X-linked 2.
Background: RBMX2 is a 322 amino acid member of the IST3 family that contains one RRM (RNA recognition motif) domain. The RBMX2 gene is intronless, conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, fruit fly, mosquito, C.elegans, S.pombe, S.cerevisiae, K.lactis, E.gossypii, M.grisea, N.crassa, A.thaliana, rice and P.falciparum, and maps to human chromosome Xq25. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions that affect males more frequently as males carry a single X chromosome.
抗原
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