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SPG11 Polyclonal antibody
SPG11 Polyclonal Antibody for IHC, ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human, mouse, rat
Applications
WB, IHC, CoIP, ELISA
Conjugate
Unconjugated
Cat no : 16555-1-AP
Synonyms
Validation Data Gallery
Tested Applications
Positive IHC detected in | human liver tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
Recommended dilution
Application | Dilution |
---|---|
Immunohistochemistry (IHC) | IHC : 1:50-1:500 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
Published Applications
KD/KO | See 2 publications below |
WB | See 6 publications below |
CoIP | See 1 publications below |
Product Information
16555-1-AP targets SPG11 in WB, IHC, CoIP, ELISA applications and shows reactivity with human, mouse, rat samples.
Tested Reactivity | human, mouse, rat |
Cited Reactivity | human, mouse |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Immunogen | SPG11 fusion protein Ag9769 |
Full Name | spastic paraplegia 11 (autosomal recessive) |
Calculated Molecular Weight | 2443 aa, 279 kDa |
GenBank Accession Number | BC024161 |
Gene Symbol | SPG11 |
Gene ID (NCBI) | 80208 |
RRID | AB_2878277 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Antigen affinity purification |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA. |
Protocols
Product Specific Protocols | |
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IHC protocol for SPG11 antibody 16555-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |
Publications
Species | Application | Title |
---|---|---|
J Clin Invest Spastic paraplegia proteins spastizin and spatacsin mediate autophagic lysosome reformation. | ||
PLoS Genet A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system. | ||
Hum Mol Genet SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction. | ||
Neurobiol Dis Loss of spatacsin function alters lysosomal lipid clearance leading to upper and lower motor neuron degeneration.
| ||
Ann Clin Transl Neurol Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11.
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