KATNA1 Antibody - #DF8027
Product: | KATNA1 Antibody |
Catalog: | DF8027 |
Description: | Rabbit polyclonal antibody to KATNA1 |
Application: | WB IHC IF/ICC |
Reactivity: | Human, Mouse, Rat |
Prediction: | Pig, Zebrafish, Bovine, Horse, Sheep, Rabbit, Dog, Chicken, Xenopus |
Mol.Wt.: | 56 kDa; 56kD(Calculated). |
Uniprot: | O75449 |
RRID: | AB_2841396 |
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Protocols
Product Info
*The optimal dilutions should be determined by the end user.
*Tips:
WB: For western blot detection of denatured protein samples. IHC: For immunohistochemical detection of paraffin sections (IHC-p) or frozen sections (IHC-f) of tissue samples. IF/ICC: For immunofluorescence detection of cell samples. ELISA(peptide): For ELISA detection of antigenic peptide.
Cite Format: Affinity Biosciences Cat# DF8027, RRID:AB_2841396.
Fold/Unfold
Katanin p60 ATPase containing subunit A1; Katanin p60 ATPase-containing subunit A1; Katanin p60 subunit A1; KATNA1; KTNA1_HUMAN; OTTHUMP00000017392; OTTHUMP00000042860; p60 katanin;
Immunogens
- O75449 KTNA1_HUMAN:
- Protein BLAST With
- NCBI/
- ExPASy/
- Uniprot
MSLLMISENVKLAREYALLGNYDSAMVYYQGVLDQMNKYLYSVKDTYLQQKWQQVWQEINVEAKHVKDIMKTLESFKLDSTPLKAAQHDLPASEGEVWSMPVPVERRPSPGPRKRQSSQYSDPKSHGNRPSTTVRVHRSSAQNVHNDRGKAVRCREKKEQNKGREEKNKSPAAVTEPETNKFDSTGYDKDLVEALERDIISQNPNVRWDDIADLVEAKKLLKEAVVLPMWMPEFFKGIRRPWKGVLMVGPPGTGKTLLAKAVATECKTTFFNVSSSTLTSKYRGESEKLVRLLFEMARFYSPATIFIDEIDSICSRRGTSEEHEASRRVKAELLVQMDGVGGTSENDDPSKMVMVLAATNFPWDIDEALRRRLEKRIYIPLPSAKGREELLRISLRELELADDVDLASIAENMEGYSGADITNVCRDASLMAMRRRIEGLTPEEIRNLSKEEMHMPTTMEDFEMALKKVSKSVSAADIERYEKWIFEFGSC
Predictions
Score>80(red) has high confidence and is suggested to be used for WB detection. *The prediction model is mainly based on the alignment of immunogen sequences, the results are for reference only, not as the basis of quality assurance.
High(score>80) Medium(80>score>50) Low(score<50) No confidence
PTMs - O75449 As Substrate
Site | PTM Type | Enzyme | Source |
---|---|---|---|
Y22 | Phosphorylation | Uniprot | |
Y29 | Phosphorylation | Uniprot | |
S42 | Phosphorylation | Q92630 (DYRK2) | Uniprot |
K44 | Ubiquitination | Uniprot | |
K51 | Ubiquitination | Uniprot | |
K71 | Ubiquitination | Uniprot | |
T72 | Phosphorylation | Uniprot | |
K77 | Ubiquitination | Uniprot | |
S80 | Phosphorylation | Uniprot | |
T81 | Phosphorylation | Uniprot | |
K84 | Ubiquitination | Uniprot | |
S93 | Phosphorylation | Uniprot | |
S109 | Phosphorylation | Q92630 (DYRK2) | Uniprot |
S118 | Phosphorylation | Uniprot | |
T133 | Phosphorylation | Q92630 (DYRK2) | Uniprot |
R148 | Methylation | Uniprot | |
K167 | Acetylation | Uniprot | |
K169 | Acetylation | Uniprot | |
S170 | Phosphorylation | Uniprot | |
T179 | Phosphorylation | Uniprot | |
K181 | Ubiquitination | Uniprot | |
S184 | Phosphorylation | Uniprot | |
K189 | Ubiquitination | Uniprot | |
K218 | Ubiquitination | Uniprot | |
K236 | Ubiquitination | Uniprot | |
K260 | Ubiquitination | Uniprot | |
K281 | Ubiquitination | Uniprot | |
S286 | Phosphorylation | Uniprot | |
Y378 | Phosphorylation | Uniprot | |
K385 | Ubiquitination | Uniprot | |
T441 | Phosphorylation | Uniprot | |
K450 | Ubiquitination | Uniprot | |
K471 | Ubiquitination | Uniprot |
Research Backgrounds
Catalytic subunit of a complex which severs microtubules in an ATP-dependent manner. Microtubule severing may promote rapid reorganization of cellular microtubule arrays and the release of microtubules from the centrosome following nucleation. Microtubule release from the mitotic spindle poles may allow depolymerization of the microtubule end proximal to the spindle pole, leading to poleward microtubule flux and poleward motion of chromosome. Microtubule release within the cell body of neurons may be required for their transport into neuronal processes by microtubule-dependent motor proteins. This transport is required for axonal growth.
Phosphorylation by DYRK2 triggers ubiquitination and subsequent degradation.
Ubiquitinated by the BCR(KLHL42) E3 ubiquitin ligase complex, leading to its proteasomal degradation. Ubiquitinated by the EDVP E3 ligase complex and subsequently targeted for proteasomal degradation.
Cytoplasm. Midbody. Cytoplasm>Cytoskeleton>Microtubule organizing center>Centrosome. Cytoplasm>Cytoskeleton>Spindle pole. Cytoplasm>Cytoskeleton>Spindle.
Note: Predominantly cytoplasmic (PubMed:9658175). Localized diffusely in the cytoplasm during the interphase (PubMed:10751153). During metaphase is localized throughout the cell and more widely dispersed than the microtubules. In anaphase and telophase is localized at the midbody region (PubMed:19261606). Also localized to the interphase centrosome and the mitotic spindle poles (By similarity). Enhanced recruitment to the mitotic spindle poles requires microtubules and interaction with KATNB1 (PubMed:10751153). Localizes within the cytoplasm, partially overlapping with microtubules, in interphase and to the mitotic spindle and spindle poles during mitosis (PubMed:26929214).
Can homooligomerize into hexameric rings, which may be promoted by interaction with microtubules. Interacts with KATNB1, which may serve as a targeting subunit. Interacts with ASPM; the katanin complex formation KATNA1:KATNB1 is required for the association of ASPM (By similarity). Interacts with dynein and NDEL1. Associates with the E3 ligase complex containing DYRK2, EDD/UBR5, DDB1 and DCAF1 proteins (EDVP complex). Interacts with KLHL42 (via the kelch domains). Interacts with CUL3; the interaction is enhanced by KLHL42. Interacts with KATNB1 and KATNBL1. Interacts with CAMSAP2 and CAMSAP3; leading to regulate the length of CAMSAP-decorated microtubule stretches.
The N-terminus is sufficient for interaction with microtubules, although high affinity binding to microtubules also requires an intact C-terminal domain and ATP, which promotes oligomerization.
Belongs to the AAA ATPase family. Katanin p60 subunit A1 subfamily.
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