Dymeclin 抗体 (AA 151-250) (AbBy Fluor® 680)
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- 抗原 See all Dymeclin (DYM) 抗体
- Dymeclin (DYM)
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抗原表位
- AA 151-250
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适用
- 人, 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 Dymeclin antibody is conjugated to AbBy Fluor® 680
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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
- 人, 大鼠
- 预测反应
- Mouse,Dog,Cow,Sheep,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Dymeclin
- 亚型
- IgG
- Top Product
- Discover our top product DYM Primary Antibody
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anti-Dymeclin (DYM) (AA 224-348) antibody
DYM 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Dymeclin (DYM) (AA 151-250) antibodyDYM 适用: 人, 大鼠 WB, ELISA, IF (cc), IF (p), ICC, IHC (fro), IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Dymeclin (DYM) (AA 343-430) antibodyDYM 适用: 人 ELISA 宿主: 小鼠 Monoclonal 1C2 unconjugated
anti-Dymeclin (DYM) (AA 546-669) antibodyDYM 适用: 人 WB, IHC, 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
- Dymeclin (DYM)
- 别名
- Dymeclin (DYM 产品)
- 别名
- DYM antibody, LOC734107 antibody, dym antibody, DMC antibody, SMC antibody, 1810041M12Rik antibody, 4933427L07Rik antibody, C030019K18Rik antibody, RGD1309111 antibody, dymeclin antibody, dymeclin L homeolog antibody, DYM antibody, dym antibody, Dym antibody, dym.L antibody
- 背景
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Synonyms: DMC, Dyggve-Melchior-Clausen syndrome protein, DYM, FLJ20071, FLJ90130, SMC, DYM_HUMAN.
Background: Dyggve-Melchior-Clausen syndrome (DMC), a rare autosomal recessive disorder, is characterized by microcephaly, short trunk dwarfism and sometime psychomotor retardation. Cutaneous cells of affected individuals show dilated rough endoplasmic reticulum and enlarged vacuoles. The Dyggve-Melchior-Clausen syndrome protein, also designated dymeclin, may play a role in proteoglycan metabolism and intracellular protein digestion. It is a widely expressed multi-pass membrane protein, detected primarily in chondrocytes and fetal brain tissue. Defects in dymeclin are also the cause of Smith-McCort dysplasis syndrome (SMC), which has characteristics identical to those of Dyggve-Melchior-Clausen syndrome.
- 基因ID
- 54808
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