Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

WHSC1 antibody (AA 525-575)

This Rabbit Polyclonal antibody specifically detects WHSC1 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN7453147

Quick Overview for WHSC1 antibody (AA 525-575) (ABIN7453147)

Target

See all WHSC1 Antibodies
WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

Reactivity

  • 22
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Human

Host

  • 19
  • 3
Rabbit

Clonality

  • 21
  • 1
Polyclonal

Conjugate

  • 12
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This WHSC1 antibody is un-conjugated

Application

  • 10
  • 5
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    AA 525-575

    Purpose

    Rabbit anti-NSD2 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 525 and 575

    Isotype

    IgG
  • Application Notes

    IP: Not recommended

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % 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

    Expiry Date

    12 months
  • Target

    WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

    Alternative Name

    NSD2

    Background

    Background: MMSET (multiple myeloma SET domain-containing protein) or NSD2 (nuclear SET-domain containing protein 2) is the product of the Wolf-Hirschhorn syndrome candidate 1 (WHSC1) gene. MMSET is a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development and is a probable histone methyltransferase. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4 [taken from NCBI Entrez Gene (Gene ID: 7468].

    Gene ID

    7468

    NCBI Accession

    NP_579877

    UniProt

    O96028

    Pathways

    SARS-CoV-2 Protein Interactome
You are here:
Chat with us!