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RBM28 antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects RBM28 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN656746

Quick Overview for RBM28 antibody (N-Term) (ABIN656746)

Target

See all RBM28 Antibodies
RBM28 (RNA Binding Motif Protein 28 (RBM28))

Reactivity

  • 22
  • 5
  • 5
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Human

Host

  • 22
Rabbit

Clonality

  • 22
Polyclonal

Conjugate

  • 17
  • 1
  • 1
  • 1
  • 1
  • 1
This RBM28 antibody is un-conjugated

Application

  • 22
  • 11
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB32488
  • Binding Specificity

    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 62-91, N-Term

    Purification

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

    Immunogen

    This RBM28 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 62-91 amino acids from the N-terminal region of human RBM28.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    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

    RBM28 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Expiry Date

    6 months
  • Target

    RBM28 (RNA Binding Motif Protein 28 (RBM28))

    Alternative Name

    RBM28

    Background

    The protein encoded by this gene is a specific nucleolar component of the spliceosomal small nuclear ribonucleoprotein (snRNP)complexes . It specifically associates with U1, U2, U4, U5, and U6 small nuclear RNAs (snRNAs), possibly coordinating their transition through the nucleolus. Mutation in this gene causes alopecia, progressive neurological defects, and endocrinopathy (ANE syndrome), a pleiotropic and clinically heterogeneous disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    85738

    Gene ID

    55131

    NCBI Accession

    NP_001159607, NP_060547

    UniProt

    Q9NW13

    Pathways

    SARS-CoV-2 Protein Interactome
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