SPP2 抗体 (AA 55-160) (AbBy Fluor® 488)
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- 抗原 See all SPP2 抗体
- SPP2 (Secreted Phosphoprotein 2 (SPP2))
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抗原表位
- AA 55-160
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适用
- 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 SPP2 antibody is conjugated to AbBy Fluor® 488
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 大鼠
- 预测反应
- Human
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SPP24/SPP2
- 亚型
- IgG
- Top Product
- Discover our top product SPP2 Primary Antibody
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anti-Secreted Phosphoprotein 2 (SPP2) (AA 55-160) antibody
SPP2 适用: 大鼠 WB, IF (cc), IF (p), IHC (p), ELISA, IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Secreted Phosphoprotein 2 (SPP2) (AA 30-211) antibodySPP2 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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
- SPP2 (Secreted Phosphoprotein 2 (SPP2))
- 别名
- SPP24 (SPP2 产品)
- 别名
- spp24 antibody, 0610038O04Rik antibody, pp-24 antibody, SPP-24 antibody, SPP24 antibody, GHRG-1 antibody, secreted phosphoprotein 2 antibody, spp2 antibody, Spp2 antibody, SPP2 antibody
- 背景
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Synonyms: SPP24, SPP-24, Secreted phosphoprotein 24, Secreted phosphoprotein 2, SPP2
Background: SPP24, also known as secreted phosphoprotein 2, is a 211 amino acid secreted protein that belongs to the cystatin superfamily. Expressed in liver and plasma, SPP24 may play a role in coordinating an aspect of bone turnover. The gene that encodes SPP24 maps to human chromosome 2, which consists of 237 million bases encoding over 1,400 genes, making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
- 基因ID
- 6694
- UniProt
- Q13103
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