C19orf21 抗体 (PE)
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北京 101111
Quick Overview for C19orf21 抗体 (PE) (ABIN2170797)
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, 小鼠, 大鼠
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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 C19orf21
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亚型
- IgG
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anti-Mitotic Spindle Positioning (MISP) (AA 63-91), (N-Term) antibody
MISP 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB25913 unconjugated
anti-Mitotic Spindle Positioning (MISP) (AA 565-614) antibodyMISP 适用: 人, 小鼠, 大鼠, Hamster, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Mitotic Spindle Positioning (MISP) (C-Term) antibodyMISP 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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FCM: (1:20-100)
Optimal working dilution should be determined by the investigator. -
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
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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- C19orf21 (MISP) (Mitotic Spindle Positioning (MISP))
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别名
- C19orf21
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背景
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Synonyms: chromosome 19 open reading frame 21, hypothetical protein LOC126353, Uncharacterized protein C19orf21, CS021_HUMAN.
Background: C19orf21 is a 679 amino acid 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
- 126353
抗原
-
