Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

RFX6 antibody

The Rabbit Polyclonal anti-RFX6 antibody has been validated for ELISA and IHC. It is suitable to detect RFX6 in samples from Human and Mouse.
Catalog No. ABIN7246697

Quick Overview for RFX6 antibody (ABIN7246697)

Target

See all RFX6 Antibodies
RFX6 (Regulatory Factor X 6 (RFX6))

Reactivity

  • 19
  • 9
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 17
  • 2
Rabbit

Clonality

  • 19
Polyclonal

Conjugate

  • 8
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This RFX6 antibody is un-conjugated

Application

  • 6
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human RFX6

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.96 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    RFX6 (Regulatory Factor X 6 (RFX6))

    Alternative Name

    RFX6

    Background

    The nuclear protein encoded by this gene is a member of the regulatory factor X (RFX) family of transcription factors. Studies in mice suggest that this gene is specifically required for the differentiation of islet cells for the production of insulin, but not for the differentiation of pancreatic polypeptide-producing cells. It regulates the transcription factors involved in beta-cell maturation and function, thus, restricting the expression of the beta-cell differentiation and specification genes. Mutations in this gene are associated with Mitchell-Riley syndrome, which is characterized by neonatal diabetes with pancreatic hypoplasia, duodenal and jejunal atresia, and gall bladder agenesis.

    UniProt

    Q8HWS3

    Pathways

    Carbohydrate Homeostasis
You are here:
Chat with us!