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HMBS antibody

The Rabbit Monoclonal anti-HMBS antibody is suitable to detect HMBS in samples from Human. It has been validated for WB.
Catalog No. ABIN7881138
$625.62
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for HMBS antibody (ABIN7881138)

Target

See all HMBS Antibodies
HMBS (Hydroxymethylbilane Synthase (HMBS))

Reactivity

  • 67
  • 36
  • 36
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 61
  • 5
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Rabbit

Clonality

  • 51
  • 16
Monoclonal

Conjugate

  • 32
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  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HMBS antibody is un-conjugated

Application

  • 44
  • 13
  • 13
  • 9
  • 7
  • 5
  • 5
  • 4
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

FEG-8
  • Purpose

    HMBS Antibody / Hydroxymethylbilane synthase

    Purification

    Affinity purified

    Immunogen

    A synthetic peptide specific to human HMBS was used as the immunogen for the HMBS antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the HMBS antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Antibody in PBS with 0.02 % sodium azide, 50 % glycerol and 0.4-0.5 mg/mL BSA

    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 the HMBS antibody at -20oC.
  • Target

    HMBS (Hydroxymethylbilane Synthase (HMBS))

    Alternative Name

    HMBS

    Background

    The HMBS gene encodes a member of the hydroxymethylbilane synthase superfamily. The encoded protein is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. Mutations in this gene are associated with the autosomal dominant disease acute intermittent porphyria. [RefSeq]

    UniProt

    P08397
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