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ZNF674 antibody (N-Term)

The Rabbit Polyclonal anti-ZNF674 antibody has been validated for WB. It is suitable to detect ZNF674 in samples from Human.
Catalog No. ABIN654866

Quick Overview for ZNF674 antibody (N-Term) (ABIN654866)

Target

See all ZNF674 Antibodies
ZNF674 (Zinc Finger Protein 674 (ZNF674))

Reactivity

  • 26
  • 1
  • 1
  • 1
Human

Host

  • 26
Rabbit

Clonality

  • 26
Polyclonal

Conjugate

  • 7
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ZNF674 antibody is un-conjugated

Application

  • 26
  • 13
  • 13
  • 10
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)

Clone

RB28735
  • Binding Specificity

    • 15
    • 7
    • 3
    • 2
    • 1
    AA 74-102, N-Term

    Purification

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

    Immunogen

    This ZNF674 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 74-102 amino acids from the N-terminal region of human ZNF674.

    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

    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

    ZNF674 (Zinc Finger Protein 674 (ZNF674))

    Alternative Name

    ZNF674

    Background

    This gene encodes a zinc finger protein with an N-terminal Kruppel-associated box-containing (KRAB) domain and 11 Kruppel-type C2H2 zinc finger domains. Like other zinc finger proteins, this gene may function as a transcription factor. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked mental retardation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq].

    Molecular Weight

    67199

    Gene ID

    641339

    NCBI Accession

    NP_001034980, NP_001139763, NP_001177346

    UniProt

    Q2M3X9
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