GTDC1 抗体 (AA 361-458) (Biotin)
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- 抗原 See all GTDC1 抗体
- GTDC1 (Glycosyltransferase-Like Domain Containing 1 (GTDC1))
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抗原表位
- AA 361-458
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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 GTDC1 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Pig,Horse,Rabbit,Zebrafish
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GTDC1
- 亚型
- IgG
- Top Product
- Discover our top product GTDC1 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
- GTDC1 (Glycosyltransferase-Like Domain Containing 1 (GTDC1))
- 别名
- GTDC1 (GTDC1 产品)
- 别名
- Hmat-Xa antibody, mat-Xa antibody, E330008O22Rik antibody, zgc:110568 antibody, glycosyltransferase like domain containing 1 antibody, glycosyltransferase-like domain containing 1 antibody, glycosyltransferase like domain containing 1 S homeolog antibody, GTDC1 antibody, Gtdc1 antibody, gtdc1.S antibody, gtdc1 antibody
- 背景
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Synonyms: Glycosyltransferase like 1, Glycosyltransferase like domain containing 1, Glycosyltransferase like domain containing protein 1, Mannosyltransferase candidate, GTDC1_HUMAN.
Background: Glycosyltransferases that mediate the regio- and stereoselective transfer of sugars, such as the fucosyltransferases, determine cell surface-carbohydrate profiles, which is an essential interface for biological recognition processes. GTDC1 (Glycosyltransferase-like domain-containing protein 1), also known as Mat-Xa, is a 458 amino acid protein belonging to the glycosyltransferase 1 family. GTDC1 is ubiquitously expressed, with highest levels found in peripheral blood leukocytes, spleen, lung and testis.An extremely rare recessive genetic disorder, Alstr syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.
- 基因ID
- 79712
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