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

SLC25A46 antibody (AA 1-50)

SLC25A46 Reactivity: Human IP Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7449139
  • Target See all SLC25A46 Antibodies
    SLC25A46 (Solute Carrier Family 25, Member 46 (SLC25A46))
    Binding Specificity
    • 6
    • 2
    • 1
    • 1
    • 1
    AA 1-50
    Reactivity
    • 14
    • 8
    • 7
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 14
    Rabbit
    Clonality
    • 14
    Polyclonal
    Conjugate
    • 10
    • 2
    • 1
    • 1
    This SLC25A46 antibody is un-conjugated
    Application
    • 10
    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunoprecipitation (IP)
    Purpose
    Rabbit anti-SLC25A46 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogen
    Between AA 1 and 50
    Isotype
    IgG
    Top Product
    Discover our top product SLC25A46 Primary Antibody
  • Application Notes
    8 - 15 μL/mg lysate
    Restrictions
    For Research Use only
  • Concentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % 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
    Expiry Date
    12 months
  • Target
    SLC25A46 (Solute Carrier Family 25, Member 46 (SLC25A46))
    Alternative Name
    SLC25A46 (SLC25A46 Products)
    Synonyms
    SLC25A46 antibody, MGC152354 antibody, zgc:92767 antibody, slc25a46 antibody, 1200007B05Rik antibody, AI325987 antibody, RGD1305072 antibody, solute carrier family 25 member 46 antibody, solute carrier family 25, member 46 antibody, solute carrier family 25 member 46 L homeolog antibody, SLC25A46 antibody, slc25a46 antibody, slc25a46.L antibody, Slc25a46 antibody
    Background
    Background: Solute carrier family 25 member 46 (SLC25A46) is a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy [taken from NCBI Entrez Gene (Gene ID: 91137)].
    Gene ID
    91137
    UniProt
    Q96AG3
You are here: