C19orf21 抗体 (Alexa Fluor 750)
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- 抗原 See all C19orf21 (MISP) products
- C19orf21 (MISP) (Mitotic Spindle Positioning (MISP))
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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 C19orf21 antibody is conjugated to Alexa Fluor 750
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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 C19orf21
- 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
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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
- C19orf21 (MISP) (Mitotic Spindle Positioning (MISP))
- 别名
- C19orf21 (MISP 产品)
- 别名
- C19orf21 antibody, 9130017N09Rik antibody, mitotic spindle positioning antibody, MISP antibody, Misp antibody
- 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.
- 基因ID
- 126353
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