Spartin (SPART) (AA 205-631) antibody (Fluoro488)

Catalog No. ABIN8041322

This Rabbit Polyclonal antibody specifically detects Spartin in FACS. It exhibits reactivity toward Human and Rat.

Quick Overview for Spartin (SPART) (AA 205-631) antibody (Fluoro488) (ABIN8041322)

Target: Spartin (SPART)

Reactivity: Human, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: Fluoro488

Application: Flow Cytometry (FACS)

Product Details

Binding Specificity: AA 205-631

Purpose: Anti-SPART Antibody Fluoro488 Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human SPART recombinant protein (Position: H205-V631).

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Expiry Date: 12 months

Target Details

Target: Spartin (SPART)

Alternative Name: SPART

Background:

Background: Spartin is a protein that in humans is encoded by the SPG20 gene. 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).

Gene Full Name: spartin

Gene ID: 23111

UniProt: Q8N0X7