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

IDS antibody (AA 1-300)

This anti-IDS antibody is a Mouse Monoclonal antibody detecting IDS in WB, IHC, ELISA and IF. Suitable for Human.
Catalog No. ABIN7115175

Quick Overview for IDS antibody (AA 1-300) (ABIN7115175)

Target

See all IDS Antibodies
IDS (Iduronate 2-Sulfatase (IDS))

Reactivity

  • 41
  • 7
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
Human

Host

  • 32
  • 10
  • 3
Mouse

Clonality

  • 38
  • 7
Monoclonal

Conjugate

  • 30
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This IDS antibody is un-conjugated

Application

  • 44
  • 17
  • 13
  • 13
  • 11
  • 8
  • 7
  • 6
  • 5
  • 5
  • 3
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Clone

2D2
  • Binding Specificity

    • 15
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-300

    Purpose

    IDS antibody

    Purification

    Protein A+G purification

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    Immunogen sequence: 1-300aa

    Immunogen: iduronate 2-sulfatase

    Isotype

    IgG1
  • Application Notes

    WB: 1:500-1:1000, IHC: 1:20-1:200, IF: 1:20-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 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.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Storage Comment

    -20°C for 12 months

    Expiry Date

    12 months
  • Target

    IDS (Iduronate 2-Sulfatase (IDS))

    Alternative Name

    IDS

    Background

    Synonyms: Iduronate 2-sulfatase|Alpha-L-iduronate sulfate sulfatase (Idursulfase)|Iduronate 2-sulfatase 42 kDa chain|Iduronate 2-sulfatase 14 kDa chain|IDS|SIDS

    Background: Iduronate 2-sulfatase (IDS) is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations causing IDS deficiency in humans result in the lysosomal storage of these glycosaminoglycans and Hunter syndrome, an X chromosome-linked disease. IDS is synthesized as two precursor forms of 76 and 90 kDa that are converted, through a 62 kDa intermediate, to 55 and 45 kDa mature polypeptides due to an internal proteolytic cleavage (PMID: 10838181).

    Molecular Weight

    76 kDa, 55 kDa

    Gene ID

    3423

    UniProt

    P22304

    Pathways

    Glycosaminoglycan Metabolic Process
You are here:
Chat with us!