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SERAC1 antibody (AA 97-623)

This Rabbit Polyclonal antibody specifically detects SERAC1 in WB, ELISA, FACS and IHC (p). It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7877273
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for SERAC1 antibody (AA 97-623) (ABIN7877273)

Target

See all SERAC1 Antibodies
SERAC1 (Serine Active Site Containing 1 (SERAC1))

Reactivity

  • 28
  • 24
  • 14
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 28
Rabbit

Clonality

  • 28
Polyclonal

Conjugate

  • 13
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
This SERAC1 antibody is un-conjugated

Application

  • 20
  • 14
  • 12
  • 10
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 12
    • 8
    • 4
    • 2
    • 2
    • 2
    • 1
    AA 97-623

    Purpose

    SERAC1 Antibody / Serine active site-containing protein 1

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids E97-H623) was used as the immunogen for the SERAC1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the SERAC1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the SERAC1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    SERAC1 (Serine Active Site Containing 1 (SERAC1))

    Alternative Name

    SERAC1

    Background

    Serine active site-containing protein 1, or Protein SERAC1 is a protein in humans that is encoded by the SERAC1 gene. The protein encoded by this gene is a phosphatidylglycerol remodeling protein found at the interface of mitochondria and endoplasmic reticula, where it mediates phospholipid exchange. The encoded protein plays a major role in mitochondrial function and intracellular cholesterol trafficking. Defects in this gene are a cause of 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (MEGDEL). Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene.

    UniProt

    Q96JX3

    Pathways

    Inositol Metabolic Process
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