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Insulin Receptor antibody (AA 1325-1358)

The Rabbit Polyclonal anti-Insulin Receptor antibody has been validated for WB. It is suitable to detect Insulin Receptor in samples from Mouse.
Catalog No. ABIN6242226

Quick Overview for Insulin Receptor antibody (AA 1325-1358) (ABIN6242226)

Target

See all Insulin Receptor (INSR) Antibodies
Insulin Receptor (INSR)

Reactivity

  • 170
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  • 16
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Mouse

Host

  • 157
  • 29
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Rabbit

Clonality

  • 144
  • 45
Polyclonal

Conjugate

  • 121
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  • 1
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  • 1
This Insulin Receptor antibody is un-conjugated

Application

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  • 13
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  • 2
  • 2
  • 2
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  • 1
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  • 1
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Western Blotting (WB)

Clone

RB50340
  • Binding Specificity

    • 16
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    • 8
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    • 2
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    • 2
    • 2
    • 2
    • 1
    • 1
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    AA 1325-1358

    Purification

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

    Immunogen

    This Mouse Insr antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 1325-1358 amino acids from Mouse Insr.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:2000. WB: 1:2000. WB: 1:2000

    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

    Expiry Date

    6 months
  • Target

    Insulin Receptor (INSR)

    Alternative Name

    Insr

    Background

    Receptor tyrosine kinase which mediates the pleiotropic actions of insulin. Binding of insulin leads to phosphorylation of several intracellular substrates, including, insulin receptor substrates (IRS1, 2, 3, 4), SHC, GAB1, CBL and other signaling intermediates. Each of these phosphorylated proteins serve as docking proteins for other signaling proteins that contain Src- homology-2 domains (SH2 domain) that specifically recognize different phosphotyrosines residues, including the p85 regulatory subunit of PI3K and SHP2. Phosphorylation of IRSs proteins lead to the activation of two main signaling pathways: the PI3K-AKT/PKB pathway, which is responsible for most of the metabolic actions of insulin, and the Ras-MAPK pathway, which regulates expression of some genes and cooperates with the PI3K pathway to control cell growth and differentiation. Binding of the SH2 domains of PI3K to phosphotyrosines on IRS1 leads to the activation of PI3K and the generation of phosphatidylinositol-(3, 4, 5)-triphosphate (PIP3), a lipid second messenger, which activates several PIP3-dependent serine/threonine kinases, such as PDPK1 and subsequently AKT/PKB. The net effect of this pathway is to produce a translocation of the glucose transporter SLC2A4/GLUT4 from cytoplasmic vesicles to the cell membrane to facilitate glucose transport. Moreover, upon insulin stimulation, activated AKT/PKB is responsible for: anti- apoptotic effect of insulin by inducing phosphorylation of BAD, regulates the expression of gluconeogenic and lipogenic enzymes by controlling the activity of the winged helix or forkhead (FOX) class of transcription factors. Another pathway regulated by PI3K- AKT/PKB activation is mTORC1 signaling pathway which regulates cell growth and metabolism and integrates signals from insulin. AKT mediates insulin-stimulated protein synthesis by phosphorylating TSC2 thereby activating mTORC1 pathway. The Ras/RAF/MAP2K/MAPK pathway is mainly involved in mediating cell growth, survival and cellular differentiation of insulin. Phosphorylated IRS1 recruits GRB2/SOS complex, which triggers the activation of the Ras/RAF/MAP2K/MAPK pathway. In addition to binding insulin, the insulin receptor can bind insulin-like growth factors (IGFI and IGFII). When present in a hybrid receptor with IGF1R, binds IGF1 (By similarity).

    Molecular Weight

    155610

    UniProt

    P15208

    Pathways

    NF-kappaB Signaling, RTK Signaling, AMPK Signaling, Carbohydrate Homeostasis, Regulation of Cell Size, Regulation of Carbohydrate Metabolic Process, Growth Factor Binding, Negative Regulation of Transporter Activity
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