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MUTED antibody (AA 40-68)

The Rabbit Polyclonal anti-MUTED antibody is suitable to detect MUTED in samples from Human and Mouse. It has been validated for WB and IHC (p).
Catalog No. ABIN654098
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$383.35
$451.00
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Quick Overview for MUTED antibody (AA 40-68) (ABIN654098)

Target

See all MUTED Antibodies
MUTED (Muted Homolog (MUTED))

Reactivity

  • 18
  • 10
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse

Host

  • 16
  • 2
Rabbit

Clonality

  • 18
Polyclonal

Conjugate

  • 9
  • 3
  • 2
  • 2
  • 1
  • 1
This MUTED antibody is un-conjugated

Application

  • 13
  • 11
  • 8
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB22107
  • Binding Specificity

    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 40-68

    Predicted Reactivity

    Pig

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This MUTED antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 40-68 amino acids from the Central region of human MUTED.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. WB: 1:1000. IHC-P: 1:50~100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    MUTED (Muted Homolog (MUTED))

    Alternative Name

    MUTED

    Background

    This gene encodes a component of BLOC-1 (biogenesis of lysosome-related organelles complex 1). Components of this complex are involved in the biogenesis of organelles such as melanosomes and platelet-dense granules. A mouse model for Hermansky-Pudlak Syndrome is mutated in the murine version of this gene. Alternative splicing results in multiple transcript variants. Read-through transcription exists between this gene and the upstream EEF1E1 (eukaryotic translation elongation factor 1 epsilon 1) gene, as well as with the downstream TXNDC5 (thioredoxin domain containing 5) gene.

    Molecular Weight

    21609

    Gene ID

    63915

    NCBI Accession

    NP_001186251, NP_958437

    UniProt

    Q8TDH9
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