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- 抗原 See all MANSC1 抗体
- MANSC1 (MANSC Domain Containing 1 (MANSC1))
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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 MANSC1 antibody is un-conjugated
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应用范围
- ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Antigen affinity purification
- 免疫原
- Fusion protein of human MANSC1
- 亚型
- IgG
- Top Product
- Discover our top product MANSC1 Primary Antibody
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anti-MANSC Domain Containing 1 (MANSC1) (AA 27-130) antibody
MANSC1 适用: 小鼠 WB, ELISA, IF (cc), IF (p), IHC (p), IHC (fro), ICC 宿主: 兔 Polyclonal unconjugated
anti-MANSC Domain Containing 1 (MANSC1) (Internal Region) antibodyMANSC1 适用: 人, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-MANSC Domain Containing 1 (MANSC1) (N-Term) antibodyMANSC1 适用: 人, Cow WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-MANSC Domain Containing 1 (MANSC1) (AA 391-419), (C-Term) antibodyMANSC1 适用: 人 WB 宿主: 兔 Polyclonal RB40891 unconjugated
anti-MANSC Domain Containing 1 (MANSC1) (N-Term) antibodyMANSC1 适用: 人, 小鼠, Cow, 大鼠, 犬, 马, 兔 WB, IHC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IHC 1:50-1:300, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1.8 mg/mL
- 缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 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
- MANSC1 (MANSC Domain Containing 1 (MANSC1))
- 别名
- MANSC1 (MANSC1 产品)
- 别名
- MANSC1 antibody, DKFZp469A172 antibody, 9130403P13Rik antibody, LOH12CR3 antibody, MANSC domain containing 1 antibody, MANSC1 antibody, Mansc1 antibody, LOC777123 antibody
- 背景
- MANSC1 (MANSC domain-containing protein 1), also known as LOH12CR3 (Loss of heterozygosity 12 chromosomal region 3 protein), is a 414 amino acid single-pass membrane protein. Expressed throughout the body, MANSC1 contains one MANSC domain and is encoded by a gene that is located on chromosome 12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.
- UniProt
- Q9H8J5
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