C19orf18 抗体
Quick Overview for C19orf18 抗体 (ABIN1385460)
抗原
适用
宿主
克隆类型
标记
应用范围
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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 C19orf18
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亚型
- IgG
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anti-Chromosome 19 Open Reading Frame 18 (C19orf18) (AA 140-168) antibody
C19orf18 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB23072 unconjugated
anti-Chromosome 19 Open Reading Frame 18 (C19orf18) (AA 147-176), (Middle Region) antibodyC19orf18 适用: 人 WB, FACS, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 19 Open Reading Frame 18 (C19orf18) (AA 35-84) antibodyC19orf18 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 19 Open Reading Frame 18 (C19orf18) (N-Term) antibodyC19orf18 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 19 Open Reading Frame 18 (C19orf18) (N-Term) antibodyC19orf18 适用: 人 WB 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
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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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- C19orf18 (Chromosome 19 Open Reading Frame 18 (C19orf18))
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别名
- C19orf18
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背景
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Synonyms: Chromosome 19 open reading frame 18, Hypothetical protein LOC1476, MGC41906, Uncharacterized protein C19orf18, CS018_HUMAN.
Background: C19orf18 is a 215 amino acid single-pass type I membrane protein that is 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.
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基因ID
- 147685
抗原
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