CACTIN 抗体 (Alexa Fluor 555)
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- 抗原 See all CACTIN 抗体
- CACTIN (Cactin, Spliceosome C Complex Subunit (CACTIN))
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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 CACTIN antibody is conjugated to Alexa Fluor 555
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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 Cactin/C19orf29
- 亚型
- IgG
- Top Product
- Discover our top product CACTIN Primary Antibody
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anti-Cactin, Spliceosome C Complex Subunit (CACTIN) (AA 460-510) antibody
CACTIN 适用: 人, Cow, 犬, 猴, Opossum, Pig WB, IHC (p), IHC 宿主: 兔 Polyclonal unconjugated
anti-Cactin, Spliceosome C Complex Subunit (CACTIN) (AA 141-190) antibodyCACTIN 适用: 人 WB, ELISA 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
- CACTIN (Cactin, Spliceosome C Complex Subunit (CACTIN))
- 别名
- C19orf29 (CACTIN 产品)
- 别名
- C19orf29 antibody, NY-REN-24 antibody, fSAPc antibody, C28H19orf29 antibody, 2510012J08Rik antibody, cactin, spliceosome C complex subunit antibody, CACTIN antibody, Cactin antibody
- 背景
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Synonyms: C19orf29, Cactin, CS029_HUMAN, FLJ17482, FLJ59622, fSAPc, Renal carcinoma antigen NY-REN-24, Uncharacterized protein C19orf29.
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 C19orf29 gene product has been provisionally designated C19orf29 pending further characterization.
- 途径
- Cellular Response to Molecule of Bacterial Origin
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