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DYH2 rabbit pAb

CAT: 0855-ES16871-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0855-ES16871-01Size:50 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. The axonemal dyneins, found in cilia and flagella, are components of the outer and inner dynein arms attached to the peripheral microtubule doublets. DNAH2 is an axonemal inner arm dynein heavy chain (Chapelin et al., 1997 [PubMed 9256245]) .[supplied by OMIM, Mar 2008]
Description
Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. The axonemal dyneins, found in cilia and flagella, are components of the outer and inner dynein arms attached to the peripheral microtubule doublets. DNAH2 is an axonemal inner arm dynein heavy chain (Chapelin et al. 1997 [PubMed 9256245]). [supplied by OMIM, Mar 2008],
UniProt
Q9P225
Swiss Prot
Q9P225
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human DYH2 AA range: 329-379
Clonality
Polyclonal
Source
Rabbit
Applications
IHC; IF
Concentration
1 mg/ml
Dilution
IHC-p 1: 50-200
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Cytoplasm, cytoskeleton, cilium axoneme . Cytoplasm, cytoskeleton, flagellum axoneme .
Gene ID (Human)
146754

UniProtKB · Q9P225

Dynein axonemal heavy chain 2

DYH2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9P225
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
DNAH2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A8K992, B5MDX5, O15434, Q6PIH3, Q6ZR42
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicingRNA editing

Ligand

ATP-bindingNucleotide-binding

Cellular component

Cell projectionCiliumCytoplasmCytoskeletonDyneinFlagellumMicrotubule

Domain

Coiled coilRepeatTPR repeat

Disease

Disease variant

Molecular function

Motor protein

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