Calcyphosine 2 抗体 (AA 221-320) (Biotin)
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- 抗原 See all Calcyphosine 2 (CAPS2) 抗体
- Calcyphosine 2 (CAPS2)
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抗原表位
- AA 221-320
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适用
- 人
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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 Calcyphosine 2 antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Pig,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Calcyphosine 2/CAPS2
- 亚型
- IgG
- Top Product
- Discover our top product CAPS2 Primary Antibody
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anti-Calcyphosine 2 (CAPS2) (AA 191-274) antibody
CAPS2 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Calcyphosine 2 (CAPS2) (AA 285-382) antibodyCAPS2 适用: 人 ELISA, WB 宿主: 小鼠 Monoclonal 3C6 unconjugated
anti-Calcyphosine 2 (CAPS2) (AA 15-89) antibodyCAPS2 适用: 小鼠 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IHC-P 1:200-400
IHC-F 1:100-500 - 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- Calcyphosine 2 (CAPS2)
- 别名
- Calcyphosine 2/CAPS2 (CAPS2 产品)
- 别名
- D630005B03Rik antibody, CAPS2 antibody, calcyphosine 2 antibody, calcyphosphine 2 antibody, CAPS2 antibody, Caps2 antibody, caps2 antibody
- 背景
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Synonyms: Calcyphosin 2, Calcyphosin-2, Calcyphosine-2, Calcyphosine2, Calcyphosphine 2, CAPS 2, CAPS2, CAYP2_HUMAN, D630005B03Rik, FLJ34520, OTTHUMP00000202412, OTTMUSP00000027695, UG0636c06.
Background: CAPS2 is a 557 amino acid calcium-binding protein that is abundantly expressed, with highest expression found in placenta, testis, colon, lung and brain. CAPS2 contains three EF-hand domains and exists as three alternatively spliced isoforms. Suggested to play a role in large dense-core vesicle (LDCV) exocytosis, CAPS2 is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
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