CXX1 抗体 (PE)
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北京 101111
Quick Overview for CXX1 抗体 (PE) (ABIN6988961)
抗原
See all CXX1 (FAM127A) 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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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 CXX1/Cerebral protein 5
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亚型
- IgG
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anti-Family with Sequence Similarity 127, Member A (FAM127A) antibody
FAM127A 适用: 人, 小鼠, 大鼠 WB, IF (p), FACS, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 127, Member A (FAM127A) (AA 1-113) antibodyFAM127A 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 127, Member A (FAM127A) (AA 1-209) antibodyFAM127A 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- FCM 1:20-100
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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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- CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
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别名
- Cerebral protein 5
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背景
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Synonyms: Mammalian retrotransposon derived protein 8C, CAAX box protein 1, Cerebral protein 5, CXX 1, FAM127A, Family with sequence similarity 127, member A, Mar8, MAR8C, Mart8, F127A_HUMAN.
Background: 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. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. 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 which affect males more frequently as males carry a single X chromosome. The CXX1 gene product has been provisionally designated CXX1 pending further characterization.
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基因ID
- 8933
抗原
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