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KTU rabbit pAb

商品貨號： PLA020286

適應(yīng) 性： 人,小鼠,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

基因名稱： DNAAF2 C14orf104 KTU
蛋白名稱： KTU
Human_gene_id： 55172
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=55172
Human_swiss_prot_no： Q9NVR5
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q9NVR5/entry
Mouse_gene_id： 109065
Mouse_gene_link： https://www.uniprot.org/uniprot/109065
Mouse_swiss_prot_no： Q8BPI1
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q8BPI1
Rat_gene_id： 362746
Rat_gene_link： https://www.uniprot.org/uniprot/362746
Rat_swiss_prot_no： Q5FVL7
Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q5FVL7
特異性： This antibody detects endogenous levels of KTU at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
分子量： 92kD
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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Cytoplasm . Dynein axonemal particle . Localizes in the apical cytoplasm around the gamma-tubulin-positive pericentriolar region, not in the cilia. .
科研貨號： PLA020286

KTU rabbit pAb

Catalog No PLA020286

Product information

基因名稱： DNAAF2 C14orf104 KTU
蛋白名稱： KTU
Human_gene_id： 55172
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=55172
Human_swiss_prot_no： Q9NVR5
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q9NVR5/entry
Mouse_gene_id： 109065
Mouse_gene_link： https://www.uniprot.org/uniprot/109065
Mouse_swiss_prot_no： Q8BPI1
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q8BPI1
Rat_gene_id： 362746
Rat_gene_link： https://www.uniprot.org/uniprot/362746
Rat_swiss_prot_no： Q5FVL7
Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q5FVL7
特異性： This antibody detects endogenous levels of KTU at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
分子量： 92kD
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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Cytoplasm . Dynein axonemal particle . Localizes in the apical cytoplasm around the gamma-tubulin-positive pericentriolar region, not in the cilia. .
科研貨號： PLA020286

Hunan UPT Biotechnology Co.,Ltd

Website：m.tjdqdt.com Servive hotline :4006916686

E-mail：service@uptbio.com

Address：

Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.

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