C19orf54 抗体 (Cy3)
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- 抗原 See all C19orf54 products
- C19orf54 (Chromosome 19 Open Reading Frame 54 (C19orf54))
- 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 C19orf54 antibody is conjugated to Cy3
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C19orf54
- 亚型
- IgG
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anti-Chromosome 19 Open Reading Frame 54 (C19orf54) (N-Term) antibody
C19orf54 适用: 人 WB 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
- C19orf54 (Chromosome 19 Open Reading Frame 54 (C19orf54))
- 别名
- C19orf54 (C19orf54 产品)
- 别名
- C19H19orf54 antibody, chromosome 19 open reading frame 54 antibody, chromosome 19 open reading frame, human C19orf54 antibody, C19orf54 antibody, C19H19orf54 antibody, c19orf54 antibody
- 背景
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Synonyms: Chromosome 19 open reading frame 54, FLJ17063, FLJ41131, Hypothetical protein LOC284325, MGC103014, UPF0692 protein C19orf54, CS054_HUMAN.
Background: C19orf54 is a 351 amino acid protein that exists as two alternatively spliced isoforms and are encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
- 基因ID
- 284325
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