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

SLC29A3 antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects SLC29A3 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5517444

Quick Overview for SLC29A3 antibody (C-Term) (ABIN5517444)

Target

See all SLC29A3 Antibodies
SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))

Reactivity

  • 14
  • 5
  • 5
  • 3
  • 3
Human

Host

  • 15
Rabbit

Clonality

  • 15
Polyclonal

Conjugate

  • 8
  • 2
  • 2
  • 1
  • 1
  • 1
This SLC29A3 antibody is un-conjugated

Application

  • 15
  • 10
  • 10
  • 3
  • 3
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    C-Term

    Sequence

    KALPGFVLLR TCLIPLFVLC NYQPRVHLKT VVFQSDVYPA LLSSLLGLSN

    Predicted Reactivity

    Dog: 86%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Rat: 86%

    Purification

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the C terminal region of human SLC29A3
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))

    Alternative Name

    SLC29A3

    Background

    This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.

    Alias Symbols: ENT3, HJCD, PHID, HCLAP

    Protein Size: 329

    Gene ID

    55315

    NCBI Accession

    XM_017016377, XP_016871866
You are here:
Chat with us!