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Rabbit anti-Human SPG20 Polyclonal Antibody

The antibody against SPG20 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-350 of human SPG20 (NP_055902.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-06997A

The antibody against SPG20 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-350 of human SPG20 (NP_055902.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-06997A ClonalityPolyclonal
Host SpeciesRabbitTarget NameSPG20
Target SynonymsSPG20; TAHCCP1FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.01% thimerosal, pH7.3.Purification MethodAffinity purification
Positive SamplesHeLa, Mouse heart, Rat brain, 293T, K-562, Mouse brain, Mouse liver, Rat lung, Rat spleenApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 1-350 of human SPG20 (NP_055902.1).Target SpeciesHuman
Uniprot IDQ8N0X7Immunogen Sequence
Background Information
  • Uniprot Id

    Q8N0X7

  • Target Species

    Human

  • Target Name

    SPART

  • Target Full Name

    Spartin

  • Target Function

    May be implicated in endosomal trafficking, or microtubule dynamics, or both. Participates in cytokinesis.

  • Target Involvement

    Spastic paraplegia 20, autosomal recessive (SPG20)

  • Target Subcellular Location

    Cytoplasm. Midbody.

  • Target Tissue Specificity

    Ubiquitously expressed, with highest levels of expression detected in adipose tissue.

  • Target Synonyms

    SPART; KIAA0610; SPG20; TAHCCP1; Spartin; Spastic paraplegia 20 protein; Trans-activated by hepatitis C virus core protein 1

  • Target 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).

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