CXX1 抗体 (AA 121-209)
Quick Overview for CXX1 抗体 (AA 121-209) (ABIN6942745)
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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抗原表位
- AA 121-209
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交叉反应
- 人
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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 Cerebral protein 5/CXX1
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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 1-209) antibodyFAM127A 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Family with Sequence Similarity 127, Member A (FAM127A) (AA 1-113) antibodyFAM127A 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. 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
- CXX1
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背景
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Synonyms: Cerebral protein 5, CAAX box protein 1, CXX 1, FAM127A, Family with sequence similarity 127, member A, Mammalian retrotransposon derived protein 8C, Mar8, MAR8C, Mart8, MART8C, CXX1_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
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UniProt
- A6ZKI3
抗原
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