SKU: WR6066 Categories: ,

U-Blot® KINH Rabbit mAb

Price range: $268.00 through $328.00

SKU: WR6066-50
Enter the quantity you would like, or drag the panel to find the quantity and price that best for you
Bulk QuoteAuthorize OEM & ODM

Product details

Background:

Specifications

Size50μL/100μL
TargetKINH
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, IF, IP, ELISA
MW(Calculated)110kD
MW(Observed)110kD
Host SpeciesRabbit
IsotypeIgG, Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:200-1:1000; WB 1:2000-1:10000; IF 1:200-1:1000; ELISA 1:5000-1:20000; IP 1:50-1:200 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationRecombinant Antibody expressed in animal component-free (ACF) media, purified via Protein A affinity chromatography.
Storage-15°C to -25°C/1 year (Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRM1964R
ImmunogenThe specific immunogen used to produce this antibody is proprietary information.
SpecificityEndogenous
Gene NameKIF5B KNS KNS1
Protein NameKINH
Other NameKinesin-1 heavy chain; / Conventional kinesin heavy chain; / Ubiquitous kinesin heavy chain; / UKHC
SpeciesHuman
Gene ID3799
UniprotP33176,
Species.1Mouse
Gene ID.116573
Uniprot.1Q61768,
Species.2Rat
Gene ID.2117550
Uniprot.2Q2PQA9
Cellular LocalizationCytoplasm , cytoskeleton . Cytolytic granule membrane . Lysosome membrane; Peripheral membrane protein; Cytoplasmic side . Uniformly distributed between soma and neurites in hippocampal neurons. .
Tissue ExpressionMuscle ,Placenta ,Uterus ,
Signaling_pathwayOrganismal Systems >> Nervous system >> Dopaminergic synapse;Human Diseases >> Cancer: specific types >> Non-small cell lung cancer;Human Diseases >> Neurodegenerative disease >> Alzheimer disease;Human Diseases >> Neurodegenerative disease >> Parkinson disease;Human Diseases >> Neurodegenerative disease >> Amyotrophic lateral sclerosis;Human Diseases >> Neurodegenerative disease >> Huntington disease;Human Diseases >> Neurodegenerative disease >> Prion disease;Human Diseases >> Neurodegenerative disease >> Pathways of neurodegeneration - multiple diseases
Research Areas>>Endocytosis; / >>Dopaminergic synapse; / >>Alzheimer disease; / >>Parkinson disease; / >>Amyotrophic lateral sclerosis; / >>Huntington disease; / >>Prion disease; / >>Pathways of neurodegeneration - multiple diseases; / >>Salmonella infection; / >>Non-small cell lung cancer
FunctionDomain:Composed of three structural domains: a large globular N-terminal domain which is responsible for the motor activity of kinesin (it hydrolyzes ATP and binds microtubule) , a central alpha-helical coiled coil domain that mediates the heavy chain dimerization; and a small globular C-terminal domain which interacts with other proteins (such as the kinesin light chains) , vesicles and membranous organelles. ,Function:Microtubule-dependent motor required for normal distribution of mitochondria and lysosomes. ,similarity:Belongs to the kinesin-like protein family. ,similarity:Belongs to the kinesin-like protein family. Kinesin subfamily. ,similarity:Contains 1 kinesin-motor domain. ,subcellular location:Uniformly distributed between soma and neurites in hippocampal neurons. ,subunit:Oligomer composed of two heavy chains and two light chains. Interacts with GRIP1 (By similarity) . Interacts with SYBU. Interacts with JAKMIP1. ,
Please login to post questions
Back to Top
Product has been added to your cart