DCTN1 Antibody

說明書

中文名稱：

DCTN1兔多克隆抗體
貨號(hào)：

CSB-PA619866ESR1HU
規(guī)格：

￥440
圖片：
Western blot
All lanes: DCTN1 antibody at 20µg/ml
Lane 1: Mouse brain tissue
Lane 2: Jurkat whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 142, 128, 137, 139, 127, 141 kDa
Observed band size: 142 kDa

Immunohistochemistry of paraffin-embedded human kidney tissue using CSB-PA619866ESR1HU at dilution of 1:100

Immunohistochemistry of paraffin-embedded human brain tissue using CSB-PA619866ESR1HU at dilution of 1:100
其他：

產(chǎn)品詳情
產(chǎn)品評(píng)價(jià)
相關(guān)產(chǎn)品
靶點(diǎn)詳情

產(chǎn)品詳情

產(chǎn)品名稱：

Rabbit anti-Homo sapiens (Human) DCTN1 Polyclonal antibody
Uniprot No.：

Q14203
基因名：

DCTN1
別名：

150 kDa dynein associated polypeptide antibody; 150 kDa dynein-associated polypeptide antibody; DAP 150 antibody; DAP-150 antibody; DAP150 antibody; DCTN 1 antibody; DCTN1 antibody; DCTN1_HUMAN antibody; DP 150 antibody; DP-150 antibody; DP150 antibody; Dynactin 1 (p150 Glued (Drosophila) homolog) antibody; Dynactin 1 (p150 glued homolog Drosophila) antibody; Dynactin 1 antibody; Dynactin subunit 1 antibody; Dynactin1 antibody; HMN7B antibody; p135 antibody; p150 Glued (Drosophila) homolog antibody; p150 glued antibody; p150 glued homolog antibody; p150(GLUED) DROSOPHILA HOMOLOG OF antibody; p150-glued antibody; p150glued antibody
宿主：

Rabbit
反應(yīng)種屬：

Human, Mouse
免疫原：

Recombinant Human Dynactin subunit 1 protein (1084-1278AA)
免疫原種屬：

Homo sapiens (Human)
標(biāo)記方式：

Non-conjugated
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

Antigen Affinity Purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
產(chǎn)品提供形式：

Liquid
應(yīng)用范圍：

ELISA, WB, IHC

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:5000
IHC	1:20-1:200

Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
Immunohistochemistry (IHC) Protocol
儲(chǔ)存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產(chǎn)品評(píng)價(jià)

靶點(diǎn)詳情

功能：

Plays a key role in dynein-mediated retrograde transport of vesicles and organelles along microtubules by recruiting and tethering dynein to microtubules. Binds to both dynein and microtubules providing a link between specific cargos, microtubules and dynein. Essential for targeting dynein to microtubule plus ends, recruiting dynein to membranous cargos and enhancing dynein processivity (the ability to move along a microtubule for a long distance without falling off the track). Can also act as a brake to slow the dynein motor during motility along the microtubule. Can regulate microtubule stability by promoting microtubule formation, nucleation and polymerization and by inhibiting microtubule catastrophe in neurons. Inhibits microtubule catastrophe by binding both to microtubules and to tubulin, leading to enhanced microtubule stability along the axon. Plays a role in metaphase spindle orientation. Plays a role in centriole cohesion and subdistal appendage organization and function. Its recruitment to the centriole in a KIF3A-dependent manner is essential for the maintenance of centriole cohesion and the formation of subdistal appendage. Also required for microtubule anchoring at the mother centriole. Plays a role in primary cilia formation.
基因功能參考文獻(xiàn)：
1. DCTN1 mutations were identified in a family with motor-neuron disease before the discovery in Perry syndrome. PMID: 28625595
2. ASK1- induced phosphorylation of EB1 not only increases its plus end-tracking ability, but also promotes its recruitment of CLIP170 and p150glued to astral microtubules. PMID: 28039481
3. DCTN1 p.K56R in patients with PSP. PMID: 27132499
4. Results suggested that variants in DCTN1 are not common risk factors for Chinese sporadic amyotrophic lateral sclerosis and that the frequency of variants of unknown significance in the cohort study was 0.39%. PMID: 28792508
5. This work reveals the structural details of Hook3's interaction with dynein and offers insight into how cargo adaptors form processive dynein-dynactin motor complexes. PMID: 27482052
6. No DCTN1 variants of disease significance were identified in this study suggesting the dynactin genes are unlikely to be a common cause of inherited peripheral neuropathies. PMID: 26662454
7. Mutations in the Dynactin 1 (DCTN1) gene have been demonstrated to result in various neurodegenerative diseases, including distal hereditary motor neuropathy type 7B. In the present study, a p.G59S mutation was identified as the underlying cause of Distal hereditary motor neuropathy type 7B in two families, and their detailed clinical features were characterized. PMID: 27573046
8. Study found that in peripheral blood mononuclear cells the median expression of KIFC3, KIF1B, and KIF5C was much lower than the expression of dynactin subunits DCTN1 and DCTN3, in both sporadic amyotrophic lateral sclerosis and healthy cases PMID: 26954557
9. Data suggest that cargo concentration at ERES is regulated by p150(glued) to coordinate protein sorting and transport carrier formation with the subsequent long-range transport towards the Golgi complex along microtubules. PMID: 26459637
10. Study shows p150glued located at the centrosome in a cell cycle-dependent manner where it is abundant during G1/S phase, located in the minus-end of microtubules during G2/M phase and at the minus-end of microtubules in the mitotic phase. PMID: 25774020
11. We find that LRRK1-mediated phosphorylation of CLIP-170 causes the accumulation of p150(Glued) (also known as DCTN1) a subunit of dynactin, at microtubule plus ends, thereby facilitating the migration of EGFR-containing endosomes. PMID: 25413345
12. The results describe the mutant dynactin p150Glued mouse model of motor neuron disease and show that genetic background influences phenotype in part through a region of chromosome 17 supporting the presence of genetic modifiers. PMID: 25763819
13. Dynactin functions as both a dynamic tether and brake during dynein-driven motility. PMID: 25185702
14. HPS6 interacts with dynactin p150Glued to mediate retrograde trafficking and maturation of lysosomes PMID: 25189619
15. Taken together, topographic and functional interactions between dynactin, importin-beta and RanBP2 are involved in nuclear translocation of IGF-1R. PMID: 24909165
16. DCTN1 mutations linked with neurogeneration on Guam. PMID: 25558820
17. The results of this study DCTN1 mutations may contribute to disparate neurodegenerative diagnoses, including familial motor neuron disease, parkinsonism, and frontotemporal atrophy. PMID: 24676999
18. The data of this study showed evidence of both striatal dopaminergic and widespread cortical/subcortical serotonergic dysfunctions in individuals carrying a mutation in the DCTN1 gene. PMID: 24797316
19. We identified 2 novel mutations of DCTN1 in patients with Perry syndrome PMID: 24484619
20. The fact that SLK (LOSK) phosphorylates only a minor isoform 1A of p150(Glued) suggests that transport and microtubule-organizing functions of dynactin are distinctly divided between the two isoforms PMID: 23985322
21. A DCTN1 point mutation was identified in a large family with progressive supranuclear palsy. PMID: 24343258
22. Data find that dynactin has multiple functions in neurons, both activating dynein-mediated retrograde axonal transport and enhancing microtubule stability through a novel anti-catastrophe mechanism regulated by tissue-specific isoform expression PMID: 23874158
23. The results of this study suggested the presence of biological changes caused by some p150 mutants pointing to a potential pathogenetic significance as modifier of the phenotype of the human disease. PMID: 23143281
24. Aurora A is involved in central spindle assembly through phosphorylation of Ser 19 in P150Glued. PMID: 23547029
25. in addition to its ciliogenic roles, Kif3a recruits p150(Glued) to the subdistal appendages of mother centrioles, critical for centrosomes to function as microtubule-organizing centres. PMID: 23386061
26. LIS1 is required for dynein-mediated transport induced by membrane tethering of BICD2-N and LIS1 contributes to dynein accumulation at microtubule plus ends and BICD2-positive cellular structures. PMID: 22956769
27. Overexpression of TBCB leads to the decreased localization of p150 to the microtubule network that might result in a functional modulation of this protein complex. PMID: 22777741
28. The tubule formations were dependent on microtubule interactions, and specifically controlled by Kif16b and dynein 1. PMID: 22357949
29. mTORC1 activation requires dynein-dependent transport to a position in the cell where it can be activated PMID: 22987636
30. Data suggest that TRAPPC9 serves to uncouple p150(Glued) from the COPII coat, and to relay the vesicle-dynactin interaction at the target membrane. PMID: 22279557
31. The p150(Glued) CAP-Gly domain regulates dynein-mediated retrograde transport at synaptic termini, and this function of dynactin is disrupted by a mutation that causes motor neuron disease. PMID: 22542187
32. End-binding proteins interact with the CAP-Gly domains of CLIP-170 and p150(glued). PMID: 22119847
33. Studies indicate that binding of dynactin, LIS1 and NudEL regulate cytoplasmic dynein motor activity. PMID: 22373868
34. Endosome movement requires an intact dynactin complex to allow p150(Glued) to activate dynein, since p50 over-expression, which disrupts the dynactin complex, inhibits inward movement even though dynein and p150(Glued) remain membrane-bound. PMID: 21915335
35. DCTN1 mutation in patients with with early stage of Perry syndrome presented with marked autonomic dysfunction including orthostatic hypotension and decreased cardiac uptake with [123]I-metaiodobenzylguanidine scintigram features PMID: 20702129
36. Par6alpha controls centrosome organization through its association with the dynactin subunit p150(Glued). PMID: 20719959
37. Data show that polo-like kinase 1 phosphorylation of p150(Glued) might be one major pathway of NEBD regulation. PMID: 20679239
38. study describes a new family carrying a G71R mutation in the DCTN1 gene; the proband displayed a series of distinctive features not previously described in Perry syndrome PMID: 20437543
39. demonstrate that the domains harboring mutated CAP-gly domains bind to microtubules but fail to bind to EB1 PMID: 20518521
40. Disruption of the SNX6-p150(Glued) interaction causes failure in formation and detachment of the tubulovesicular sorting structures from endosomes and results in block of CI-MPR retrieval from endosomes to the TGN. PMID: 19935774
41. DCTN1 subunit p150Glued isoforms notable for differential interaction with microtubules. PMID: 19778315
42. Genomic organization of the DCTN1-SLC4A5 locus encoding both NBC4 and p150(Glued). PMID: 12063394
43. dysfunction of dynactin-mediated transport can lead to human motor neuron disease PMID: 12627231
44. neither APC nor p150glued binding domain is necessary for EB1 or EBF3 to induce microtubule bundling PMID: 14514668
45. role in extension and assembly of adherens junctions in photoreceptor development PMID: 15067220
46. Heterozygous missense mutations of DCTN1 were found in a sporadic case of ALS (T1249I), 1 pt with familial ALS (M571T), two pts with familial ALS, & two unaffected relatives (R785W). Alleleic variants of DCTN1 may be a genomic risk factor for ALS. PMID: 15326253
47. The R1101K sequence alteration of the DCTN1 gene may predispose subjects to ALS and FTD. PMID: 16240349
48. The Gly59Ser mutation disrupts folding of the cytoskeleton-associated protein glycine-rich (CAP-Gly) domain, resulting in aggregation of p150Glued protein in vitro and in vivo, accompanied by an increase in cell death in a motor neuron cell line. PMID: 16505168
49. The function of p150(Glued) in membrane trafficking is not associated with plus-end localization. PMID: 16772339
50. Dynactin p150(Glued) plays an important role in the functional integrity of the keratinocyte microparasol. PMID: 17344930
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相關(guān)疾病：

Neuronopathy, distal hereditary motor, 7B (HMN7B); Amyotrophic lateral sclerosis (ALS); Perry syndrome (PERRYS)
亞細(xì)胞定位：

Cytoplasm. Cytoplasm, cytoskeleton. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriole. Cytoplasm, cytoskeleton, spindle. Nucleus envelope. Cytoplasm, cell cortex.
蛋白家族：

Dynactin 150 kDa subunit family
組織特異性：

Brain.
數(shù)據(jù)庫(kù)鏈接：

HGNC: 2711

OMIM: 105400

KEGG: hsa:1639

STRING: 9606.ENSP00000354791

UniGene: Hs.516111

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