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RBM10 antibody (AA 1-180)

The Rabbit Polyclonal anti-RBM10 antibody has been validated for WB. It is suitable to detect RBM10 in samples from Human.
Catalog No. ABIN1682489

Quick Overview for RBM10 antibody (AA 1-180) (ABIN1682489)

Target

See all RBM10 Antibodies
RBM10 (RNA Binding Motif Protein 10 (RBM10))

Reactivity

  • 35
  • 14
  • 12
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
Human

Host

  • 34
  • 2
Rabbit

Clonality

  • 34
  • 2
Polyclonal

Conjugate

  • 21
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This RBM10 antibody is un-conjugated

Application

  • 22
  • 18
  • 11
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-180

    Sequence

    MEYERRGGRG DRTGRYGATD RSQDDGGENR SRDHDYRDMD YRSYPREYGS QEGKHDYDDS SEEQSAEDSY EASPGSETQR RRRRRHRHSP TGPPGFPRDG DYRDQDYRTE QGEEEEEEED EEEEEKASNI VMLRMLPQAA TEDDIRGQLQ SHGVQAREVR LMRNKSSGQS RGFAFVEFSH

    Cross-Reactivity

    Human

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human RBM10 (NP_005667.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • 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

    RBM10 (RNA Binding Motif Protein 10 (RBM10))

    Alternative Name

    RBM10

    Background

    This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.,RBM10,DXS8237E,GPATC9,GPATCH9,S1-1,TARPS,ZRANB5,Epigenetics & Nuclear Signaling,RNA Binding,RBM10

    Molecular Weight

    94 kDa/103 kDa

    Gene ID

    8241

    UniProt

    P98175
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