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Invitrogen
SPG11 Polyclonal Antibody
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Product Details
PA5-59366
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit
/ IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human SPG11. Recombinant protein control fragment (Product #RP-98054).
Conjugate
Form
Liquid
Concentration
0.2 mg/mL
Amount
20 µg
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.2, with 40% glycerol
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
Product Specific Information
Immunogen sequence: RLHNMKLSIS YLRECAKAND WLQFIIHSQL HNYHPAEVKS LIQYFSPVIQ DHLRLAFENL PSVPTSKMDS DQVCNKCPQE LQGSKQEMTD LFEILLQCS
Highest antigen sequence identity to the following orthologs: Mouse - 65%, Rat - 66%.
Target Information
Hereditary spastic paraplegias (HSPs) are genetically and phenotypically heterogeneous disorders. Spastic paraplegia with thinning of the corpus callosum (ARHSP-TCC) is a relatively frequent form of complicated hereditary spastic paraplegia (cHSP) in which mental retardation and muscle stiffness at onset are followed by slowly progressive paraparesis and cognitive deterioration. Mutations of the SPG11 gene encoding the spatacsin protein have been identified as a major cause of HSP-TCC. Spatacsin is a potential transmembrane protein that is phosphorylated upon DNA damage. It is expressed in all structures of the brain, with a high expression in the cerebellum. SPG11 mutations may occur more frequently in familial than sporadic forms of cHSP without TCC. Kjellin syndrome is found to be associated with mutations in not only the SPG15 gene but also SPG11 gene. Recent studies show Parkinsonism may initiate SPG11-linked HSP TCC and that SPG11 may cause juvenile Parkinsonism.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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Bioinformatics
Protein Aliases: amyotrophic lateral sclerosis 5; Colorectal carcinoma-associated protein; spastic paraplegia 11 (autosomal recessive); Spastic paraplegia 11 protein; Spatacsin; SPG11, spatacsin vesicle trafficking associated; unnamed protein product
Gene Aliases: ALS5; CMT2X; KIAA1840; SPG11
UniProt ID: (Human) Q96JI7
Entrez Gene ID: (Human) 80208
protein import into nucleus
intracellular protein transport
lysosome organization
chemical synaptic transmission
axonogenesis
neuromuscular junction development
memory
axo-dendritic transport
protein localization
corticospinal tract morphogenesis
protein catabolic process
cholesterol efflux
vesicle transport along microtubule
synaptic vesicle transport
axon extension
skeletal muscle fiber development
neuron apoptotic process
localization within membrane
motor behavior
phagosome-lysosome fusion involved in apoptotic cell clearance
walking behavior
motor neuron apoptotic process
autophagosome organization
regulation of store-operated calcium entry
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Performance Guarantee
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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