C19orf24 抗体
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- 抗原 See all C19orf24 products
- C19orf24 (Chromosome 19 Open Reading Frame 24 (C19orf24))
- 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 C19orf24 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (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 C19orf24
- 亚型
- IgG
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anti-Chromosome 19 Open Reading Frame 24 (C19orf24) (N-Term) antibody
C19orf24 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 19 Open Reading Frame 24 (C19orf24) (N-Term) antibodyC19orf24 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 19 Open Reading Frame 24 (C19orf24) (N-Term) antibodyC19orf24 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 19 Open Reading Frame 24 (C19orf24) antibodyC19orf24 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- C19orf24 (Chromosome 19 Open Reading Frame 24 (C19orf24))
- 别名
- C19orf24 (C19orf24 产品)
- 别名
- chromosome 19 open reading frame 24 antibody, C19orf24 antibody, c19orf24 antibody
- 背景
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Synonyms: C19orf24, Chromosome 19 open reading frame 24, CS024_HUMAN, FLJ20640, Hypothetical protein LOC55009, Uncharacterized membrane protein C19orf24.
Background: Consisting of around 63 million bases with over 1,400 genes, chromosome 19 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. The C19orf24 gene product has been provisionally designated C19orf24 pending further characterization.
- 基因ID
- 55009
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