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RIN2 antibody

This anti-RIN2 antibody is a Rabbit Polyclonal antibody detecting RIN2 in WB. Suitable for Human and Mouse.
Catalog No. ABIN6568165

Quick Overview for RIN2 antibody (ABIN6568165)

Target

See all RIN2 Antibodies
RIN2 (Ras and Rab Interactor 2 (RIN2))

Reactivity

  • 9
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Mouse

Host

  • 5
  • 4
Rabbit

Clonality

  • 6
  • 3
Polyclonal

Conjugate

  • 9
This RIN2 antibody is un-conjugated

Application

  • 9
  • 5
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Purification

    Affinity purification

    Immunogen

    Recombinant protein of human RIN2

    Isotype

    IgG
  • Application Notes

    WB 1:500 - 1:2000

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    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

    RIN2 (Ras and Rab Interactor 2 (RIN2))

    Alternative Name

    RIN2

    Background

    Synonyms: MACS ,RAB5 interacting protein 2,Ras and Rab interactor 2,RAS association (RalGDS/AF-6) domain containing protein JC265,Ras association domain family 4,Ras inhibitor JC265,Ras interaction/interference protein 2,RASSF4,RIN 2,RIN2,RIN2

    Background: The RAB5 protein is a small GTPase involved in membrane trafficking in the early endocytic pathway. The protein encoded by this gene binds the GTP-bound form of the RAB5 protein preferentially over the GDP-bound form, and functions as a guanine nucleotide exchange factor for RAB5. The encoded protein is found primarily as a tetramer in the cytoplasm and does not bind other members of the RAB family. Mutations in this gene cause macrocephaly alopecia cutis laxa and scoliosis (MACS) syndrome, an elastic tissue disorder, as well as the related connective tissue disorder, RIN2 syndrome. Alternative splicing results in multiple transcript variants.

    Molecular Weight

    Observed_MW: 120kDa

    Calculated_MW: 100kDa/105kDa

    Gene ID

    54453

    UniProt

    Q8WYP3
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