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TSFM anticorps (AA 1-325)

L’anticorps Lapin Polyclonal anti-TSFM a été validé pour WB et ELISA. Il convient pour détecter TSFM dans des échantillons de Humain.
N° du produit ABIN7599272

Aperçu rapide pour TSFM anticorps (AA 1-325) (ABIN7599272)

Antigène

Voir toutes TSFM Anticorps
TSFM (Ts Translation Elongation Factor, Mitochondrial (TSFM))

Reactivité

  • 30
  • 11
  • 10
  • 6
  • 5
  • 5
  • 5
  • 3
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 28
  • 3
Lapin

Clonalité

  • 25
  • 6
Polyclonal

Conjugué

  • 26
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TSFM est non-conjugé

Application

  • 30
  • 13
  • 6
  • 6
  • 4
  • 3
  • 2
Western Blotting (WB), ELISA
  • Épitope

    • 8
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-325

    Fonction

    Anti-EF-Ts/TSFM Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-EF-Ts/TSFM Antibody Picoband® (ABIN7599272). Tested in ELISA, WB applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human EF-Ts/TSFM recombinant protein (Position: M1-E325).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.25-0.5 μg/mL, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Ahola, S., Isohanni, P., Euro, L., Brilhante, V., Palotie, A., Pihko, H., Lonnqvist, T., Lehtonen, T., Laine, J., Tyynismaa, H., Suomalainen, A. Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophy. Neurology 83: 743-751, 2014. 2. Shamseldin, H. E., Alshammari, M., Al-Sheddi, T., Salih, M. A., Alkhalidi, H., Kentab, A., Repetto, G. M., Hashem, M., Alkuraya, F. S. Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes. J. Med. Genet. 49: 234-241, 2012. 3. Smeitink, J. A. M., Elpeleg, O., Antonicka, H., Diepstra, H., Saada, A., Smits, P., Sasarman, F., Vriend, G., Jacob-Hirsch, J., Shaag, A., Rechavi, G., Welling, B., Horst, J., Rodenburg, R. J., van den Heuvel, B., Shoubridge, E. A. Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs. Am. J. Hum. Genet. 79: 869-877, 2006.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Antigène

    TSFM (Ts Translation Elongation Factor, Mitochondrial (TSFM))

    Autre désignation

    TSFM

    Sujet

    Synonyms: Annexin A8 ,Annexin VIII ,Annexin-8 ,Vascular anticoagulant-beta ,VAC-beta ,ANXA8 ,ANX8,

    Tissue Specificity: Ubiquitously expressed.

    Background: Elongation factor Ts, mitochondrial is a protein that in humans is encoded by the TSFM gene. It is an EF-Ts homolog. This gene encodes a mitochondrial translation elongation factor. The encoded protein is an enzyme that catalyzes the exchange of guanine nucleotides on the translation elongation factor Tu during the elongation step of mitchondrial protein translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-3 syndrome. Alternate splicing results in multiple transcript variants.

    Poids moléculaire

    35 kDa

    ID gène

    10102

    UniProt

    P43897
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