DENND2C 抗体
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- 抗原 See all DENND2C products
- DENND2C (DENN/MADD Domain Containing 2C (DENND2C))
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适用
- 人, 小鼠
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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 DENND2C antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human DENND2C
- 亚型
- IgG
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anti-DENN/MADD Domain Containing 2C (DENND2C) (AA 1-300) antibody
DENND2C 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-DENN/MADD Domain Containing 2C (DENND2C) (AA 359-408) antibodyDENND2C 适用: 人, 小鼠, 大鼠, 兔, 犬, 马, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- DENND2C (DENN/MADD Domain Containing 2C (DENND2C))
- 别名
- DENND2C (DENND2C 产品)
- 别名
- si:dkeyp-46c9.6 antibody, MGC145874 antibody, dJ1156J9.1 antibody, A930010I20Rik antibody, RGD1308197 antibody, DENN domain containing 2C antibody, DENN/MADD domain containing 2C antibody, DENND2C antibody, dennd2c antibody, Dennd2c antibody
- 背景
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Synonyms: DENN/MADD domain containing 2C, dJ1156J9.1, DKFZp686G0351, DKFZp686N1631, DKFZp779P1149, FLJ37099, RP5-1156J9.1, DEN2C_HUMAN.
Background: DENND2C is a 928 amino acid protein that contains a dDENN domain, a DENN domain, and a uDENN domain and exists as three isoforms as a result of alternative splicing. The DENND2C protein is thought to target to actin filaments and control Rab9-dependent trafficking of mannose-6-phosphate receptor to lysosomes. The gene encoding DENND2C maps to human chromosome 1, the largest human chromosome which spans about 260 million base pairs and makes up 8 % of the human genome. Other notable genes located on chromosome 1 include LMNA, which is associated with the rare aging disease Hutchinson-Gilford progeria, and the MUTYH gene, which is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome.
- 基因ID
- 163259
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