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SCCPDH antibody

This Rabbit Polyclonal antibody specifically detects SCCPDH in WB. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN7260229

Quick Overview for SCCPDH antibody (ABIN7260229)

Target

See all SCCPDH Antibodies
SCCPDH (Saccharopine Dehydrogenase (SCCPDH))

Reactivity

  • 17
  • 11
  • 11
  • 3
  • 3
  • 2
  • 2
  • 1
Human, Mouse

Host

  • 15
  • 2
Rabbit

Clonality

  • 17
Polyclonal

Conjugate

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SCCPDH antibody is un-conjugated

Application

  • 10
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human SCCPDH (NP_057086.2).

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 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.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    SCCPDH (Saccharopine Dehydrogenase (SCCPDH))

    Alternative Name

    SCCPDH

    Background

    SCCPDH (Probable saccharopine dehydrogenase) is a 429 amino acid protein that belongs to the saccharopine dehydrogenase family. The SCCPDH gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, fruit fly, mosquito and C.elegans, and maps to human chromosome 1q44. 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. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

    Molecular Weight

    Observed_MW: 45 kDa

    Calculated_MW: 47 kDa

    Gene ID

    51097

    UniProt

    Q8NBX0

    Pathways

    SARS-CoV-2 Protein Interactome
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