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DCTN1 Antibody, Cy5 Conjugated

DCTN1 Antibody, Cy5 Conjugated size: 0.1ml 350

Supplier BIOSS PRIMARY CONJUGATED ANTIBODIES 1
Price 350
Size 0.1ml
Contact us Ask Component cell markers and DNA bp. markers are genetic markerser genes or DNA sequenceswith selection audit
Long name Cy5 Conjugated, DCTN1 Polyclonal Antibody
CategoryConjugated Primary Antibodies
Conjugation5, Cy5
Host OrganismRabbit (Oryctolagus cuniculus)
Target AntigenDCTN1
SpecificityThis is a highly specific antibody against DCTN1
ModificationUnmodified
Modification siteNone
ClonalityPolyclonal
ClonePolyclonal antibody
Concentration1ug per 1ul
SourceKLH conjugated synthetic peptide derived from human DCTN1/Dynactin 1
Gene ID number1639
Tested applicationsIF(IHC-P)
Recommended dilutionsIF(IHC-P)(1:50-200)
Crossreactivity Mouse, Rat, Human
Crossreactive species details not every possible cross-reactivity is known, Due to limited amount of testing and knowledge
Antigen background ALS is a neurodegenerative disorder affecting upper and lower motor neurons, Brain, Death usually occurs within 2 to 5 years, Defects in DCTN1 are the cause of distal hereditary motor neuronopathy type 7B (HMN7B), Distal hereditary motor neuronopathies constitute a heterogeneous group of neuromuscular disorders caused by selective degeneration of motor neurons in the anterior horn of the spinal cord, Dynein-dynactin interaction is a key component of the mechanism of axonal transport of vesicles and organelles, HMN7B is a neuromuscular disorder, Later on, Parkinsonism develops later and respiratory failure occurred terminally, Perry syndrome is a neuropsychiatric disorder characterized by mental depression not responsive to antidepressant drugs or electroconvulsive therapy, Sensory abnormalities are absent, The disease starts with weakness and wasting of distal muscles of the anterior tibial and peroneal compartments of the legs, The etiology is likely to be multifactorial, The overall clinical picture consists of a classical distal muscular atrophy syndrome in the legs without clinical sensory loss, also called parkinsonism with alveolar hypoventilation and mental depression, also known as progressive lower motor neuron disease (PLMND), and resulting in fatal paralysis, exhaustion and marked weight loss, involving both genetic and environmental factors, sleep disturbances, weakness and atrophy may expand to the proximal muscles of the lower limbs and/or to the distal upper limbs, without sensory deficit in the posterior horn, Defects in DCTN1 are a cause of susceptibility to amyotrophic lateral sclerosis (ALS), Defects in DCTN1 are the cause of Perry syndrome (PERRYS), Involvement in disease, Required for the cytoplasmic dynein-driven retrograde movement of vesicles and organelles along microtubules, Tissue specificity
Purification methodThis antibody was purified via Protein A
Storage conditions 50% glycerol and 0, Store refrigerated at 2 to 8 degrees Celcius for up to 1 year, 09% sodium azide, Keep the antibody in an aqueous buffered solution containing 1% BSA
Excitation Emission625, 650nm/670nm
Properties Cy5 antibodies are excited by the 650-nanometer wave of an argon laser and detected at a 670-nanometer captor, C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies they should be stored frozen at - 24°
Gene targetDCTN1 Conjugated
Short name Conjugated, DCTN1 Antibody
Technique antibodies against human proteins, antibodies for, antibody Conjugates, Antibody
LabelCy5
Alternative name cyanine 5 coupled, DCTN1 (Antibody to)
Alternative techniqueantibodies
Identity 2711
Gene DCTN1
Long gene name dynactin subunit 1
Synonyms gene name Glued (Drosophila) homolog) , dynactin 1 (p150
Synonyms name p150 glued homolog (Drosophila)
Locus 2p13, 1
Discovery year 1995-10-03
Entrez gene record 1639
Pubmed identfication 1828535
RefSeq identity NM_004082
Classification Dynactin
Havana BLAST/BLAT OTTHUMG00000129963
Locus Specific Databases Inherited Peripheral Neuropathies Mutation Database ALSOD, the Amyotrophic Lateral Sclerosis Online Genetic Database LRG_237

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