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RGS antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects RGS in WB and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN5532989

Quick Overview for RGS antibody (N-Term) (ABIN5532989)

Target

See all RGS Antibodies
RGS (Regulator of G-Protein Signaling 9 (RGS))

Reactivity

  • 25
  • 10
  • 8
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
Human

Host

  • 28
Rabbit

Clonality

  • 28
Polyclonal

Conjugate

  • 22
  • 2
  • 1
  • 1
  • 1
  • 1
This RGS antibody is un-conjugated

Application

  • 27
  • 21
  • 13
  • 7
  • 6
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 8
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 149-178, N-Term

    Purification

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

    Immunogen

    This RGS9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 149-178 amino acids from the N-terminal region of human RGS9.

    Isotype

    Ig Fraction
  • Application Notes

    For WB starting dilution is: 1:1000

    For IHC-P starting dilution is: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.35 mg/mL

    Buffer

    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

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    RGS (Regulator of G-Protein Signaling 9 (RGS))

    Alternative Name

    RGS9

    Background

    This gene encodes a member of the RGS family of GTPase activating proteins that function in various signaling pathways by accelerating the deactivation of G proteins. This protein is anchored to photoreceptor membranes in retinal cells and deactivates G proteins in the rod and cone phototransduction cascades. Mutations in this gene result in bradyopsia. Multiple transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    77 kDa

    Gene ID

    8787

    UniProt

    O75916

    Pathways

    Myometrial Relaxation and Contraction, Regulation of G-Protein Coupled Receptor Protein Signaling, Phototransduction
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