SCFD2 抗体 (AA 501-600) (Biotin)
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- 抗原 See all SCFD2 抗体
- SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))
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抗原表位
- AA 501-600
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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 SCFD2 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 预测反应
- Dog,Cow,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SCFD2
- 亚型
- IgG
- Top Product
- Discover our top product SCFD2 Primary Antibody
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- 应用备注
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WB 1:300-5000
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
- SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))
- 别名
- SCFD2 (SCFD2 产品)
- 别名
- STXBP1L1 antibody, 9330137G15 antibody, E430013M20Rik antibody, sec1 family domain containing 2 antibody, Sec1 family domain containing 2 antibody, Scfd2 antibody, SCFD2 antibody
- 背景
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Synonyms: FLJ21060, FLJ39514, SCFD 2, Scfd2, SCFD2_HUMAN, Sec1 family domain containing 2, Sec1 family domain containing protein 2, Sec1 family domain-containing protein 2, STXBP1L1, Syntaxin binding protein 1 like 1, Syntaxin-binding protein 1-like 1.
Background: SCFD2 is a 684 amino acid protein suggested to play a role in protein transport. Existing as two alternatively spliced isoforms, SCFD2 is a member of the STXBP/unc-18/SEC1 family and is encoded by a gene that maps to human chromosome 4q12. Chromosome 4 represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
- 基因ID
- 152579
- UniProt
- Q8WU76
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