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The antibody against TPP1 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 284-563 of human TPP1 (NP_000382.3) 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 TPP1 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 284-563 of human TPP1 (NP_000382.3) 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-10800A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | TPP1 |
| Target Synonyms | CLN2; GIG1; LPIC; SCAR7; TPP-1; TPP1 | Form | Liquid |
| Species Reactivity | Human, Mouse | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | BT-474, SW480 | Application | ELISA, WB |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 284-563 of human TPP1 (NP_000382.3). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | O14773 | Immunogen Sequence |
Uniprot Id
O14773
Target Species
Human
Target Name
TPP1
Target Full Name
Tripeptidyl-peptidase 1
Target Function
Lysosomal serine protease with tripeptidyl-peptidase I activity. May act as a non-specific lysosomal peptidase which generates tripeptides from the breakdown products produced by lysosomal proteinases. Requires substrates with an unsubstituted N-terminus.
Target Involvement
Ceroid lipofuscinosis, neuronal, 2 (CLN2); Spinocerebellar ataxia, autosomal recessive, 7 (SCAR7)
Target Subcellular Location
Lysosome. Melanosome.
Target Tissue Specificity
Detected in all tissues examined with highest levels in heart and placenta and relatively similar levels in other tissues.
Target Synonyms
Cell growth inhibiting gene 1 protein; Cell growth-inhibiting gene 1 protein; Ceroid lipofuscinosis neuronal 2; Ceroid lipofuscinosis neuronal 2 late infantile (Jansky Bielschowsky disease); Ceroid lipofuscinosis neuronal 2 late infantile; CLN 2; CLN2; GIG 1; GIG1; Growth inhibiting protein 1; LPIC; Lysosomal pepstatin insensitive protease; Lysosomal pepstatin-insensitive protease; MGC21297; TPP 1; TPP I; TPP-1; TPP-I; Tpp1; TPP1_HUMAN; TPPI; Tripeptidyl aminopeptidase; Tripeptidyl peptidase I; Tripeptidyl-peptidase 1; Tripeptidyl-peptidase I
Target Background
This gene encodes a member of the sedolisin family of serine proteases. The protease functions in the lysosome to cleave N-terminal tripeptides from substrates, and has weaker endopeptidase activity. It is synthesized as a catalytically-inactive enzyme which is activated and auto-proteolyzed upon acidification. Mutations in this gene result in late-infantile neuronal ceroid lipofuscinosis, which is associated with the failure to degrade specific neuropeptides and a subunit of ATP synthase in the lysosome.
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