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KTU Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT6786
产品名称
KTU Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
DNAAF2 C14orf104 KTU
蛋白名称
KTU
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
55172
Human Gene Link
https://www.uniprot.org/uniprot/55172
Human Swissprot No.
Q9NVR5
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q9NVR5/entry
Mouse Gene ID
109065
Mouse Gene Link
https://www.uniprot.org/uniprot/109065
Mouse Swissprot No.
Q8BPI1
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/Q8BPI1
Rat Gene ID
362746
Rat Gene Link
https://www.uniprot.org/uniprot/362746
Rat Swissprot No.
Q5FVL7
Rat Swissprot Link
https://www.uniprot.org/uniprotkb/Q5FVL7
免疫原
Synthesized peptide derived from human KTU AA range: 610-660
特异性
This antibody detects endogenous levels of KTU at Human/Mouse/Rat
稀释度
WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
参考分子量
92kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a highly conserved protein involved in the preassembly of dynein arm complexes which power cilia. These complexes are found in some cilia and are assembled in the cytoplasm prior to transport for cilia formation. Mutations in this gene have been associated with primary ciliary dyskinesia. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009],
细胞定位
Cytoplasm . Dynein axonemal particle . Localizes in the apical cytoplasm around the gamma-tubulin-positive pericentriolar region, not in the cilia. .
功能
disease:Defects in KTU are the cause of primary ciliary dyskinesia type 10 (CILD10) [MIM:612518]. CILD 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 abnormalities of sperm tails. Half of the patients exhibit situs inversus, due to dysfunction of monocilia at the embryonic node and randomization of left-right body asymmetry. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome.,function:Required for cytoplasmic pre-assembly of axonemal dyneins, thereby playing a central role in motility in cilia and flagella. Involved in pre-assembly of dynein arm complexes in the cytoplasm before intraflagellar transport loads them for the ciliary compartment.,similarity:Belongs to the PIH1 family. Kintoun subfamily.,subcellular location:Localizes in the apical cytoplasm around the gamma-tubulin-positive pericentriolar region, not in the cilia.,subunit:Interacts with DNAI2 and HSPA1A.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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