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CNNM4 antibody (C-Term)

This anti-CNNM4 antibody is a Rabbit Polyclonal antibody detecting CNNM4 in WB. Suitable for Human.
Catalog No. ABIN657513

Quick Overview for CNNM4 antibody (C-Term) (ABIN657513)

Target

See all CNNM4 Antibodies
CNNM4 (Cyclin M4 (CNNM4))

Reactivity

  • 25
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 26
Rabbit

Clonality

  • 26
Polyclonal

Conjugate

  • 13
  • 3
  • 3
  • 3
  • 2
  • 2
This CNNM4 antibody is un-conjugated

Application

  • 22
  • 18
  • 8
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

RB32844
  • Binding Specificity

    • 7
    • 7
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 501-530, C-Term

    Purification

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

    Immunogen

    This CNNM4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 501-530 amino acids from the C-terminal region of human CNNM4.

    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

    CNNM4 Antibody (C-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

    CNNM4 (Cyclin M4 (CNNM4))

    Alternative Name

    CNNM4

    Background

    This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta. [provided by RefSeq].

    Molecular Weight

    86607

    Gene ID

    26504

    NCBI Accession

    NP_064569

    UniProt

    Q6P4Q7
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