CXorf56 抗体 (AA 120-170) (Alexa Fluor 594)
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- 抗原 See all CXorf56 (CXORF56) 抗体
- CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))
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抗原表位
- AA 120-170
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适用
- 人, 小鼠, 大鼠
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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 CXorf56 antibody is conjugated to Alexa Fluor 594
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CXorf56
- 亚型
- IgG
- Top Product
- Discover our top product CXORF56 Primary Antibody
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anti-Chromosome X Open Reading Frame 56 (CXORF56) (AA 1-222) antibody
CXORF56 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Chromosome X Open Reading Frame 56 (CXORF56) (AA 120-170) antibodyCXORF56 适用: 人, 小鼠, 大鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 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
- CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))
- 别名
- CXorf56 (CXORF56 产品)
- 别名
- C4HXorf56 antibody, CXorf56 antibody, c330007p06-a antibody, cxorf56 antibody, chromosome X open reading frame 56 antibody, chromosome 4 CXorf56 homolog antibody, chromosome X open reading frame, human CXorf56 antibody, RIKEN cDNA C330007P06 gene antibody, chromosome X open reading frame 56 L homeolog antibody, CXorf56 antibody, C4HXorf56 antibody, CXHXorf56 antibody, C330007P06Rik antibody, cxorf56.L antibody
- 背景
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Synonyms: UPF0428 protein CXorf56, CXorf56
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 CXorf56 gene product has been provisionally designated CXorf56 pending further characterization.
- 基因ID
- 63932
- UniProt
- Q9H5V9
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