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Anti-RNF186 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Anti-RNF186 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
# de catalogue 10670-254
Fournisseur:  Bioss
Anti-RNF186 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
# de catalogue 10670-254
Fournisseur:  Bioss
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Spécifications

  • Antibody type:
    Primary
  • Antigen name:
    Ring Finger Protein 186
  • Clonality:
    Polyclonal
  • Gene ID:
    54546
  • Host:
    Rabbit
  • Isotype:
    IgG
  • Reactivity:
    Human,
    Rat,
    Mouse
  • Antigen symbol:
    RNF186
  • Conjugation:
    HRP (Horseradish Peroxidase)
  • ImmunoChemistry:
    Yes
  • Size:
    100 µL
  • Western blot:
    Yes
  • Cross adsorption:
    No
  • Form:
    liquid
  • Antigen synonyms:
    Ring finger protein 186|RNF 186|FLJ20225|RN186_HUMAN.|RP11 91K11.1
  • Storage buffer:
    Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% Gentamicin. Store at 4°C for 12 months.
  • Storage temperature:
    Store at –20 °C for 12 months
  • Concentration:
    1 μg/μl
  • Shipping temperature:
    4°C
  • Purification:
    Purified by Protein A
  • Cat. no.:
    10670-254
  • Supplier No.:
    BS-9262R-HRP

Spécifications

A propos de cet article

The RING finger motif is a specialized DNA-binding zinc finger domain found in many transcriptional regulatory proteins. The ring finger protein (RNF) family includes any protein containing the signature RING finger motif. RNF186 (RING finger protein 186) is a 227 amino acid multi-pass membrane protein containing one RING-type zinc finger. The gene encoding RNF186 maps to human chromosome 1p36.13. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.

Recommended Dilutions: Western Blot: 1:100-1000; IHC-P: 1:100-500

Type: Primary
Antigen: RNF186
Clonality: Polyclonal
Clone:
Conjugation: HRP (Horseradish Peroxidase)
Epitope:
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat

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