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MKS1 antibody

This Rabbit Polyclonal antibody specifically detects MKS1 in WB and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN7469490
$740.00
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 3 to 5 Business Days

Quick Overview for MKS1 antibody (ABIN7469490)

Target

See all MKS1 Antibodies
MKS1 (Meckel Syndrome, Type 1 (MKS1))

Reactivity

  • 11
  • 2
  • 2
Human

Host

  • 11
Rabbit

Clonality

  • 11
Polyclonal

Conjugate

  • 11
This MKS1 antibody is un-conjugated

Application

  • 9
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Cross-Reactivity

    Human, Rat

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human MKS1. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: Jurkat

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.63 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    MKS1 (Meckel Syndrome, Type 1 (MKS1))

    Alternative Name

    MKS1

    Background

    Synonyms: MKS transition zone complex subunit 1 , BBS13 , JBTS28 , MES , MKS , POC12

    Background: The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]

    Molecular Weight

    65 kDa

    Gene ID

    54903

    UniProt

    Q9NXB0
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