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
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
Tested Application Dilution
ICC/IFAssay - dependent
WB1 - 3 µg/ml
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
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

GeneID: 23111 Human SPG20

Swiss-port # Q8N0X7 Human Spartin

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.