SPAST rabbit pAb

SPAST rabbit pAb

AO-06-ES12999-50

SPAST rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES12999
Product nameSPAST rabbit pAb
ReactivityHuman; Mouse;Rat
ApplicationsWB
Other name
Size50μL
Unit price ($)148
Human gene ID6683
Human Swiss-ProtQ9UBP0
SourceRabbit
IsotypeIgG
TargetSPAST
Fields
Gene nameSPAST ADPSP FSP2 KIAA1083 SPG4
Protein nameSPAST
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID50850
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9QYY8
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID362700
Rat gene linkView Rat Gene
Rat Swiss-ProtB2RYN7
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from human SPAST AA range: 163-213
SpecificityThis antibody detects endogenous levels of SPAST at Human/Mouse/Rat
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)68kD
Observed band (KD)
BackgroundThis gene encodes a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. The encoded ATPase may be involved in the assembly or function of nuclear protein complexes. Two transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their full length sequences have not been determined. Mutations associated with this gene cause the most frequent form of autosomal dominant spastic paraplegia 4. [provided by RefSeq, Jul 2008],
Functionalternative products:Alternative promoter usage of a cryptic promoter in exon 1 can direct the synthesis of N-terminally truncated isoforms, which may also arise from alternative initiation,catalytic activity:ATP + H(2)O = ADP + phosphate.,developmental stage:Expressed in fetal brain, heart, kidney, liver, lung, skeletal muscle, spleen and thymus.,disease:Defects in SPAST are the cause of spastic paraplegia autosomal dominant type 4 (SPG4) [MIM:182601]. Spastic paraplegia is a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the w
Subcellular locationMembrane ; Peripheral membrane protein . Endoplasmic reticulum . Midbody . Cytoplasm, cytoskeleton, microtubule organizing center, centrosome . Cytoplasm, cytoskeleton . Cytoplasm, perinuclear region . Nucleus . Cytoplasm, cytoskeleton, spindle . Cytoplasm . Forms an intramembrane hairpin-like structure in the membrane (PubMed:20200447). Localization to the centrosome is independent of microtubules (PubMed:15891913). Localizes to the midbody of dividing cells, and this requires CHMP1B (PubMed:18997780). Enriched in the distal axons and branches of postmitotic neurons (PubMed:15269182). .; [Isoform 1]: Endoplasmic reticulum membrane ; Peripheral membrane protein . Nucleus membrane . Lipid droplet . Cytoplasm, cytoskeleton . Endosome . Forms an intramembrane hairpin-like structure in the mem
ExpressionExpressed in brain, heart, kidney, liver, lung, pancreas, placenta and skeletal muscle. The short isoforms may predominate in brain and spinal cord.

Additional Images

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Western blot analysis of lysates from KB cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES12999-50
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