ARG65128
anti-SPARTIN antibody
anti-SPARTIN antibody for ICC/IF,Western blot and Human
Cell Biology and Cellular Response antibody; Gene Regulation antibody
Overview
Product Description | Goat Polyclonal antibody recognizes SPARTIN |
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Tested Reactivity | Hu |
Tested Application | ICC/IF, WB |
Host | Goat |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | SPARTIN |
Antigen Species | Human |
Immunogen | C-EASGTDVKQLDQGNK |
Conjugation | Un-conjugated |
Alternate Names | Spastic paraplegia 20 protein; SPARTIN; Trans-activated by hepatitis C virus core protein 1; Spartin; TAHCCP1 |
Application Instructions
Application Suggestion |
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Application Note | WB: Recommend incubate at RT for 1h. * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
Form | Liquid |
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Purification | Purified from goat serum by antigen affinity chromatography. |
Buffer | Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA. |
Preservative | 0.02% Sodium azide |
Stabilizer | 0.5% BSA |
Concentration | 0.5 mg/ml |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
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Background | This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome). [provided by RefSeq, Nov 2008] |
Research Area | Cell Biology and Cellular Response antibody; Gene Regulation antibody |
Calculated MW | 73 kDa |
PTM | Ubiquitinated; ubiquitination does not require ITCH and WWP1. |