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- 文献和实验
- 技术资料
- 免疫原:
Recombinant Human Microcephalin protein (536-835AA)
- 亚型:
IgG
- 形态:
Liquid
- 保存条件:
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性:
Polyclonal
- 标记物:
Non-conjugated
- 适应物种:
Human
- 保质期:
6个月
- 抗原来源:
Homo sapiens (Human)
- 目录编号:
Q8NEM0
- 级别:
优
- 库存:
200
- 供应商:
武汉华美生物工程有限公司
- 宿主:
Rabbit
- 应用范围:
ELISA, WB, IHC, IF; Recommended dilution: WB:1:500-1:2000, IHC:1:20-1:200, IF:1:50-1:200
- 浓度:
>95%,Antigen Affinity Purified
- 靶点:
MCPH1
- 抗体英文名:
MCPH1 Antibody
- 抗体名:
Microcephaly primary autosomal recessive 1 antibody
- 规格:
100μl/50μl/20μl
| 规格: | 100μl | 产品价格: | ¥1320.0 |
|---|---|---|---|
| 规格: | 50μl | 产品价格: | ¥880.0 |
| 规格: | 20μl | 产品价格: | ¥440.0 |
保存缓冲液
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.功能
Implicated in chromosome condensation and DNA damage induced cellular responses. May play a role in neurogenesis and regulation of the size of the cerebral cortex.风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验A 腺苷脱氨酶缺乏症 adenosine deaminase deficiency (ADA) 腺病毒 adenovirus Alagille综合征 Alagille syndrome 等位基因 allele 氨基酸 amino acids 动物模型 animal model 抗体 antibody 凋亡 apoptosis 路-巴综合征 ataxia-telangiectasia 常染色体显性 autosomal dominant 常染色体 autosome B
needed for the biosynthesis of glucocorticoids and mineralocorticoids. Manifestations are usually present at birth or during early childhood, but symptoms may appear later in life in nonclassic CAH. CAH is uncommon and often has an autosomal recessive
, nonmalignant pain should be assessed and treated in a stepped approach. Measures include: nonpharmacologic methods, such as heat, ice, elevation, and rest acetaminophen (Tylenol) nonsteroidal anti-inflammatories
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