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TSFM antibody (AA 1-325)

The Rabbit Polyclonal anti-TSFM antibody has been validated for WB and ELISA. It is suitable to detect TSFM in samples from Human.
Catalog No. ABIN7599272

Quick Overview for TSFM antibody (AA 1-325) (ABIN7599272)

Target

See all TSFM Antibodies
TSFM (Ts Translation Elongation Factor, Mitochondrial (TSFM))

Reactivity

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

Host

  • 28
  • 3
Rabbit

Clonality

  • 25
  • 6
Polyclonal

Conjugate

  • 26
  • 1
  • 1
  • 1
  • 1
  • 1
This TSFM antibody is un-conjugated

Application

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

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

    Purpose

    Anti-EF-Ts/TSFM Antibody Picoband®

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    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.

    Immunogen

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

    Isotype

    IgG
  • Application Notes

    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.

    Storage

    4 °C,-20 °C

    Storage Comment

    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.
  • Target

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

    Alternative Name

    TSFM

    Background

    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.

    Molecular Weight

    35 kDa

    Gene ID

    10102

    UniProt

    P43897
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