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The antibody against SPG11 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 550-750 of human SPG11 (NP_079413.3) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
The antibody against SPG11 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 550-750 of human SPG11 (NP_079413.3) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
| Cat.No | ADA-01425A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | SPG11 |
| Target Synonyms | ALS5; CMT2X; KIAA1840; SPG11 | Form | Liquid |
| Species Reactivity | Human | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | U-87MG | Application | ELISA, WB |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 550-750 of human SPG11 (NP_079413.3). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | Q96JI7 | Immunogen Sequence |
Uniprot Id
Q96JI7
Target Species
Human
Target Name
SPG11
Target Full Name
Spatacsin
Target Function
May play a role in neurite plasticity by maintaining cytoskeleton stability and regulating synaptic vesicle transport.
Target Involvement
Spastic paraplegia 11, autosomal recessive (SPG11); Amyotrophic lateral sclerosis 5, juvenile (ALS5); Charcot-Marie-Tooth disease 2X (CMT2X)
Target Subcellular Location
Cytoplasm, cytosol. Nucleus. Cell projection, axon. Cell projection, dendrite.
Target Tissue Specificity
Expressed in all structures of brain, with a high expression in cerebellum. Expressed in cortical projection neurons.
Target Synonyms
Colorectal carcinoma associated protein; Colorectal carcinoma-associated protein; DKFZp762B1512; FLJ21439; KIAA1840; Spastic paraplegia 11 (autosomal recessive); Spastic paraplegia 11; Spastic paraplegia 11 protein; Spatacsin; SPG 11; Spg11; SPTCS_HUMAN
Target Background
The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene.
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