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Dynein IC1 Rabbit pAb

-YT1429

Catalog: YT1429
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
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40μL
$150.00
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Main Information
Target

Dynein IC1

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, ELISA

MW

79kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-1:2000; ELISA 1:20000; Not yet tested in other applications.
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
Dynein IC1 Polyclonal Antibody detects endogenous levels of Dynein IC1 protein.
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
79kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
The antiserum was produced against synthesized peptide derived from human DNAI1. AA range:211-260
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Specificity:
Dynein IC1 Polyclonal Antibody detects endogenous levels of Dynein IC1 protein.
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Gene Name:
DNAI1
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Protein Name:
Dynein intermediate chain 1 axonemal
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Other Name:
DNAI1 ;
Dynein intermediate chain 1 ;
axonemal ;
Axonemal dynein intermediate chain 1
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Database Link:
Organism Gene ID SwissProt
Human 27019; Q9UI46;
Mouse 68922; Q8C0M8;
Rat 500442; Q5XIL8;
Background:
This gene encodes a member of the dynein intermediate chain family. The encoded protein is part of the dynein complex in respiratory cilia. The inner- and outer-arm dyneins, which bridge between the doublet microtubules in axonemes, are the force-generating proteins responsible for the sliding movement in axonemes. The intermediate and light chains, thought to form the base of the dynein arm, help mediate attachment and may also participate in regulating dynein activity. Mutations in this gene result in abnormal ciliary ultrastructure and function associated with primary ciliary dyskinesia and Kartagener syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013],
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Function:
Disease:Defects in DNAI1 are the 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 DNAI1 are the cause of primary ciliary dyskinesia type 1 (CILD1) [MIM:244400]. CILD1 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:Part of the dynein complex of respiratory cilia.,similarity:Belongs to the dynein intermediate chain family.,similarity:Contains 5 WD repeats.,subunit:Consists of at least two heavy chains and a number of intermediate and light chains.,
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Cellular Localization:
Dynein axonemal particle . Cytoplasm, cytoskeleton, cilium axoneme .
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Tissue Expression:
Expressed in respiratory ciliated cells (at protein level).
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Research Areas:
>>Amyotrophic lateral sclerosis ;
>>Huntington disease ;
>>Pathways of neurodegeneration - multiple diseases
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Catalog: YT1429
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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