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DYH5 rabbit pAb

说明书

BYab-08986

  • 20UL ¥460 50UL ¥945 100UL ¥1350
  • 货期: 3天左右

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宿主
反应性
应用
IHC;IF
分子量(DA)
免疫原
Synthesized peptide derived from human DYH5 AA range: 2445-2495
特异性
This antibody detects endogenous levels of DYH5 at Human/Mouse
来源
Polyclonal, Rabbit,IgG
组成(Formulation)
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
稀释比例
IHC-p 1:50-200. IF 1:50-200
纯化工艺(Immunogen)
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
浓度
1 mg/ml
背景(Background)
This gene encodes a dynein protein, which is part of a microtubule-associated motor protein complex consisting of heavy, light, and intermediate chains. This protein is an axonemal heavy chain dynein. It functions as a force-generating protein with ATPase activity, whereby the release of ADP is thought to produce the force-producing power stroke. Mutations in this gene cause primary ciliary dyskinesia type 3, as well as Kartagener syndrome, which are both diseases due to ciliary defects. [provided by RefSeq, Oct 2009],
功能
disease:Defects in DNAH5 are a cause of Kartagener syndrome (KTGS) [MIM:244400]. KTGS is an autosomal recessive disorder characterized by the association of primary ciliary dyskinesia with situs inversus. Clinical features include recurrent respiratory infections, bronchiectasis, infertility, and lateral transposition of the viscera of the thorax and abdomen. The situs inversus is most often total, although it can be partial in some cases (isolated dextrocardia or isolated transposition of abdominal viscera).,disease:Defects in DNAH5 are the cause of primary ciliary dyskinesia type 3 (CILD3) [MIM:608644]. CILD3 is an autosomal recessive disorder characterized by axonemal abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to
基因名称(Gene Name)
DNAH5 DNAHC5 HL1 KIAA1603
蛋白名称
DYH5
简称
DYH5
其他名称
Fields
>>Amyotrophic lateral sclerosis;>>Huntington disease;>>Pathways of neurodegeneration - multiple diseases
人基因ID
1767
人蛋白质序列数据库
Q8TE73
小鼠基因ID
110082
小鼠蛋白质序列数据库
Q8VHE6
大鼠基因ID
大鼠蛋白质序列数据库
细胞定位
Cytoplasm, cytoskeleton, cilium axoneme .
组织表达
Expressed in airway epithelial cells (at protein level). Not detected in spermatozoa (at protein level).
储存(Storage)
-20°C/1 year

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DYH5 rabbit pAb

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