MOSPD2 抗体 (AA 111-496) (Biotin)
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北京 101111
Quick Overview for MOSPD2 抗体 (AA 111-496) (Biotin) (ABIN8011686)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 111-496
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原理
- Anti-MOSPD2 Antibody Biotin Conjugated
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human MOSPD2 recombinant protein (Position: R111-Q496).
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亚型
- IgG
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anti-Motile Sperm Domain Containing 2 (MOSPD2) (AA 11-40), (N-Term) antibody
MOSPD2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB33344 unconjugated
anti-Motile Sperm Domain Containing 2 (MOSPD2) (Middle Region) antibodyMOSPD2 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.
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有效期
- 12 months
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- MOSPD2 (Motile Sperm Domain Containing 2 (MOSPD2))
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别名
- MOSPD2
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背景
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Background: MOSPD2 (motile sperm domain-containing protein 2) is a 518 amino acid single-pass membrane protein that contains one CRAL-TRIO domain and a single MSP domain. Existing as two alternatively spliced isoforms, MOSPD2 is encoded by a gene that maps to human chromosome Xp22.2. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Gene Full Name: motile sperm domain containing 2
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基因ID
- 158747
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UniProt
- Q8NHP6
抗原
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