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HMGCL antibody (N-Term)

The Rabbit Polyclonal anti-HMGCL antibody has been validated for WB. It is suitable to detect HMGCL in samples from Human.
Catalog No. ABIN1539566

Quick Overview for HMGCL antibody (N-Term) (ABIN1539566)

Target

See all HMGCL Antibodies
HMGCL (3-Hydroxymethyl-3-Methylglutaryl-CoA Lyase (HMGCL))

Reactivity

  • 50
  • 32
  • 10
  • 6
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 66
  • 2
Rabbit

Clonality

  • 63
  • 5
Polyclonal

Conjugate

  • 35
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HMGCL antibody is un-conjugated

Application

  • 58
  • 29
  • 15
  • 13
  • 13
  • 9
  • 8
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB22965
  • Binding Specificity

    • 15
    • 10
    • 7
    • 7
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 71-99, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This HMGCL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 71-99 amino acids from the N-terminal region of human HMGCL.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    HMGCL Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • Target

    HMGCL (3-Hydroxymethyl-3-Methylglutaryl-CoA Lyase (HMGCL))

    Alternative Name

    HMGCL

    Background

    The protein encoded by this gene belongs to the HMG-CoA lyase family. It is a mitochondrial enzyme that catalyzes the final step of leucine degradation and plays a key role in ketone body formation. Mutations in this gene are associated with HMG-CoA lyase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq].

    Molecular Weight

    34360

    Gene ID

    3155

    NCBI Accession

    NP_000182, NP_001159531

    UniProt

    P35914
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