CXX1 抗体 (AA 121-209) (Alexa Fluor 488)
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- 抗原 See all CXX1 (FAM127A) 抗体
- CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
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抗原表位
- AA 121-209
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This CXX1 antibody is conjugated to Alexa Fluor 488
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应用范围
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Cerebral protein 5/CXX1
- 亚型
- IgG
- Top Product
- Discover our top product FAM127A Primary Antibody
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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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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
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
- 别名
- CXX1 (FAM127A 产品)
- 别名
- CXX1 antibody, MAR8C antibody, MART8C antibody, Mar8 antibody, Mart8 antibody, retrotransposon Gag like 8C antibody, RTL8C antibody
- 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.
- 基因ID
- 8933
- UniProt
- A6ZKI3
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