Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

PTDSS1 antibody (AA 1-70)

This anti-PTDSS1 antibody is a Rabbit Polyclonal antibody detecting PTDSS1 in WB. Suitable for Human.
Catalog No. ABIN6146381

Quick Overview for PTDSS1 antibody (AA 1-70) (ABIN6146381)

Target

See all PTDSS1 Antibodies
PTDSS1 (phosphatidylserine Synthase 1 (PTDSS1))

Reactivity

  • 32
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 30
  • 2
Rabbit

Clonality

  • 32
Polyclonal

Conjugate

  • 12
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PTDSS1 antibody is un-conjugated

Application

  • 23
  • 17
  • 9
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 6
    • 3
    • 3
    • 2
    • 1
    AA 1-70

    Sequence

    MASCVGSRTL SKDDVNYKMH FRMINEQQVE DITIDFFYRP HTITLLSFTI VSLMYFAFTR DDSVPEDNIW

    Cross-Reactivity

    Human

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-70 of human PTDSS1 (NP_055569.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

    PTDSS1 (phosphatidylserine Synthase 1 (PTDSS1))

    Alternative Name

    PTDSS1

    Background

    The protein encoded by this gene catalyzes the formation of phosphatidylserine from either phosphatidylcholine or phosphatidylethanolamine. Phosphatidylserine localizes to the mitochondria-associated membrane of the endoplasmic reticulum, where it serves a structural role as well as a signaling role. Defects in this gene are a cause of Lenz-Majewski hyperostotic dwarfism. Two transcript variants encoding different isoforms have been found for this gene.,PTDSS1,LMHD,PSS1,PSSA,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,PTDSS1

    Molecular Weight

    56 kDa

    Gene ID

    9791

    UniProt

    P48651
You are here:
Chat with us!