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Antibody Product Overview
| ELK.No | ES7177 |
| Product name | Dynein IC2 rabbit pAb |
| Reactivity | Human;Mouse;Rat;Chicken |
| Applications | WB;ELISA |
| Other name | DNAI2; Dynein intermediate chain 2; axonemal; Axonemal dynein intermediate chain 2 |
| Size | 100μL |
| Unit price ($) | 248 |
| Human gene ID | 64446 |
| Human Swiss-Prot | Q9GZS0 |
| Source | Rabbit |
| Isotype | IgG |
| Target | Dynein IC2 |
| Fields | >>Amyotrophic lateral sclerosis;>>Huntington disease;>>Pathways of neurodegeneration - multiple diseases |
| Gene name | DNAI2 |
| Protein name | Dynein intermediate chain 2 axonemal |
| Human gene link | View Human Gene |
| Human Swiss link | View Human Swiss-Prot |
| Mouse gene ID | 432611 |
| Mouse gene link | View Mouse Gene |
| Mouse Swiss-Prot | A2AC93 |
| Mouse Swiss link | View Mouse Swiss-Prot |
| Rat gene ID | 360654 |
| Rat gene link | View Rat Gene |
| Rat Swiss-Prot | Q66HC9 |
| Rat Swiss link | View Rat Swiss-Prot |
| Immunogen | The antiserum was produced against synthesized peptide derived from human DNAI2. AA range:71-120 |
| Specificity | Dynein IC2 Polyclonal Antibody detects endogenous levels of Dynein IC2 protein. |
| Formulation | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
| Clonality | Polyclonal |
| Dilution | Western Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications. |
| Purification | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
| Concentration | 1 mg/ml |
| Storage stability | -20°C/1 year |
| Molecular Weight (Da) | |
| Observed band (KD) | 70kD |
| Background | The protein encoded by this gene belongs to the dynein intermediate chain family, and is part of the dynein complex of respiratory cilia and sperm flagella. Mutations in this gene are associated with primary ciliary dyskinesia type 9. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Mar 2010], |
| Function | disease:Defects in DNAI2 are the cause of primary ciliary dyskinesia type 9 (CILD9) [MIM:612444]. 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:Part of the dynein complex of respiratory cilia.,sequence caution:Intron retention.,similarity:Belongs to the dynein intermediate chain family.,similarity:Contains 5 WD repeats.,subunit:Consists of at least two heavy chains and a nu |
| Subcellular location | Cytoplasm, cytoskeleton, cilium axoneme . Dynein axonemal particle . Located in the proximal region of respiratory cilia. . |
| Expression | Highly expressed in trachea and testis. Expressed in respiratory ciliated cells (at protein level) (PubMed:33139725). |
Additional Images
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Western blot analysis of DNAI2 Antibody. The lane on the right is blocked with the DNAI2 peptide.
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Western blot analysis of the lysates from RAW264.7cells using DNAI2 antibody.
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: AO-06-ES7177-100
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