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SIM1 antibody (N-Term)

The Rabbit Polyclonal anti-SIM1 antibody has been validated for WB, IHC (p) and EIA. It is suitable to detect SIM1 in samples from Human.
Catalog No. ABIN954809

Quick Overview for SIM1 antibody (N-Term) (ABIN954809)

Target

See all SIM1 Antibodies
SIM1 (Single-Minded Homolog 1 (SIM1))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This SIM1 antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
  • Binding Specificity

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    AA 1-30, N-Term

    Specificity

    This antibody recongnizes Human SIM1 (N-term).

    Purification

    Protein A column, followed by peptide affinity purification

    Immunogen

    KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of Human SIM1 Genename: SIMI1

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    SIM1 (Single-Minded Homolog 1 (SIM1))

    Alternative Name

    SIM1

    Background

    SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or mental retardation of Down syndrome.Synonyms: BHLHE14, Class E basic helix-loop-helix protein 14, Single-minded homolog 1

    Molecular Weight

    85515 Da

    Gene ID

    6492

    NCBI Accession

    NP_005059
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