SKU: WP3673 Categories: ,

KINH rabbit pAb

Price range: $268.00 through $328.00

SKU: WP3673-100
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
MW(Calculated)
MW(Observed)105kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human KINH AA range: 64-114
SpecificityThis antibody detects endogenous levels of KINH at Human/Mouse/Rat
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