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- 抗原 See all GJC2 抗体
- GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
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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 GJC2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- A synthetic peptide of human GJC2
- 亚型
- IgG
- Top Product
- Discover our top product GJC2 Primary Antibody
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anti-Gap Junction Protein, gamma 2, 47kDa (GJC2) (Middle Region) antibody
GJC2 适用: 人, 兔 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Gap Junction Protein, gamma 2, 47kDa (GJC2) (N-Term) antibodyGJC2 适用: 人 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Gap Junction Protein, gamma 2, 47kDa (GJC2) (N-Term) antibodyGJC2 适用: 人 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Gap Junction Protein, gamma 2, 47kDa (GJC2) antibodyGJC2 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Gap Junction Protein, gamma 2, 47kDa (GJC2) (C-Term) antibodyGJC2 适用: 人, 兔, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Gap Junction Protein, gamma 2, 47kDa (GJC2) (AA 21-70) antibodyGJC2 适用: 人 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500-1:2000 IHC 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: 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. Avoid freeze / thaw cycles.
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- 抗原
- GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
- 别名
- GJC2 (GJC2 产品)
- 别名
- GJA12 antibody, cx47 antibody, gja12 antibody, cx46.6 antibody, pmldar antibody, MGC146420 antibody, B230382L12Rik antibody, Cx47 antibody, Gja12 antibody, CX46.6 antibody, HLD2 antibody, LMPH1C antibody, PMLDAR antibody, SPG44 antibody, gap junction protein gamma 2 antibody, si:dkey-91f15.1 antibody, gap junction protein, gamma 2 antibody, GJC2 antibody, gjc2 antibody, si:dkey-91f15.1 antibody, Gjc2 antibody
- 背景
- This gene encodes a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1.
- 分子量
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Observed_MW: 47 kDa
Calculated_MW: 47 kDa
- 基因ID
- 57165
- UniProt
- Q5T442
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