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NBPF3 antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects NBPF3 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5517639

Quick Overview for NBPF3 antibody (N-Term) (ABIN5517639)

Target

See all NBPF3 Antibodies
NBPF3 (Neuroblastoma Breakpoint Family, Member 3 (NBPF3))

Reactivity

Human

Host

  • 7
Rabbit

Clonality

  • 7
Polyclonal

Conjugate

  • 3
  • 2
  • 1
  • 1
This NBPF3 antibody is un-conjugated

Application

  • 5
  • 3
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 5
    • 1
    • 1
    N-Term

    Sequence

    CDQVKKEDQE ATSPRLSREL LDEKEPEVLQ DSLDRFYSTP FEYLELPDLC

    Predicted Reactivity

    Human: 100%

    Characteristics

    This is a rabbit polyclonal antibody against NBPF3. It was validated on Western Blot.

    Purification

    Affinity Purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N-terminal region of Human NBPF3
  • 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

    NBPF3 (Neuroblastoma Breakpoint Family, Member 3 (NBPF3))

    Alternative Name

    NBPF3

    Background

    This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. DUF1220 copy number variations in human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, mental retardation, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes.

    Alias Symbols: NBPF3, L7,

    Protein Interaction Partner: NBPF3, APP, UBD, UBC, TSEN15, ANK1, EWSR1,

    Protein Size: 275

    Gene ID

    84224
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