CSAD 抗体 (AA 401-493) (AbBy Fluor® 555)
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- 抗原 See all CSAD 抗体
- CSAD (Cysteine Sulfinic Acid Decarboxylase (CSAD))
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抗原表位
- AA 401-493
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适用
- 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 CSAD antibody is conjugated to AbBy Fluor® 555
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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
- 小鼠, 大鼠
- 预测反应
- Human,Dog,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CSAD
- 亚型
- IgG
- Top Product
- Discover our top product CSAD Primary Antibody
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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
- CSAD (Cysteine Sulfinic Acid Decarboxylase (CSAD))
- 别名
- CSAD (CSAD 产品)
- 别名
- zgc:103478 antibody, Ci-CSD antibody, CSD antibody, PCAP antibody, Csd antibody, cysteine sulfinic acid decarboxylase antibody, csad antibody, csd antibody, PSHAa2293 antibody, CpipJ_CPIJ010964 antibody, VDBG_07509 antibody, PSM_A0793 antibody, CSAD antibody, Csad antibody
- 背景
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Synonyms: CSAD, CSAD_HUMAN, CSD, Cysteine sulfinic acid decarboxylase, Cysteine-sulfinate decarboxylase, Sulfinoalanine decarboxylase.
Background: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD 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.
- 基因ID
- 51380
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