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WDR4 antibody

The Mouse Monoclonal anti-WDR4 antibody is suitable to detect WDR4 in samples from Human. It has been validated for WB, IF and FACS.
Catalog No. ABIN2735512
$608.40
Plus shipping costs $50.00
0.1 mL
Shipping to: United States
Delivery in 6 to 9 Business Days

Quick Overview for WDR4 antibody (ABIN2735512)

Target

See all WDR4 Antibodies
WDR4 (WD Repeat Domain 4 (WDR4))

Reactivity

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  • 1
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Human

Host

  • 42
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Mouse

Clonality

  • 29
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Monoclonal

Conjugate

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  • 2
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  • 2
  • 2
  • 2
  • 1
  • 1
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This WDR4 antibody is un-conjugated

Application

  • 36
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  • 1
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)

Clone

4G1
  • Characteristics

    Homo sapiens WD repeat domain 4 (WDR4), transcript variant 2

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Full length human recombinant protein of human WDR4(NP_387510) produced in HEK293T cell.

    Isotype

    IgG1
  • Application Notes

    WB 1:2000, IF 1:100, FLOW 1:100,

    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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

    -20 °C
  • Target

    WDR4 (WD Repeat Domain 4 (WDR4))

    Alternative Name

    WDR4

    Background

    This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Two transcript variants encoding the same protein have been found for this gene.

    Molecular Weight

    45.3 kDa

    Gene ID

    10785

    NCBI Accession

    NM_033661

    HGNC

    10785
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