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NSUN5 antibody (AA 277-466)

This anti-NSUN5 antibody is a Rabbit Polyclonal antibody detecting NSUN5 in WB and IHC. Suitable for Human.
Catalog No. ABIN7268955

Quick Overview for NSUN5 antibody (AA 277-466) (ABIN7268955)

Target

See all NSUN5 Antibodies
NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))

Reactivity

  • 24
  • 2
  • 1
Human

Host

  • 24
Rabbit

Clonality

  • 24
Polyclonal

Conjugate

  • 7
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NSUN5 antibody is un-conjugated

Application

  • 21
  • 13
  • 13
  • 10
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 5
    • 1
    • 1
    • 1
    AA 277-466

    Purpose

    NSUN5 Rabbit pAb

    Sequence

    SCCELAEEDF LAVSPSDPRY HEVHYILLDP SCSGSGMPSR QLEEPGAGTP SPVRLHALAG FQQRALCHAL TFPSLQRLVY STCSLCQEEN EDVVRDALQQ NPGAFRLAPA LPAWPHRGLS TFPGAEHCLR ASPETTLSSG FFVAVIERVE VPSSASQAKA SAPERTPSPA PKRKKRQQRA AAGACTPPCT

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 277-466 of human NSUN5 (NP_683759.1).

    Isotype

    IgG
  • Application Notes

    WB,1:200 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))

    Alternative Name

    NSUN5

    Background

    This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms.,NSUN5,NOL1,NOL1R,NSUN5A,WBSCR20,WBSCR20A,p120,p120(NOL1),Epigenetics & Nuclear Signaling,RNA Binding,Signal Transduction,Endocrine & Metabolism,NSUN5

    Molecular Weight

    36kDa/42kDa/46kDa/50kDa/51kDa

    Gene ID

    55695

    UniProt

    Q96P11
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