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NPHP3 antibody (AA 1092-1142)

The Rabbit Polyclonal anti-NPHP3 antibody is suitable to detect NPHP3 in samples from Human and Mouse. It has been validated for WB.
Catalog No. ABIN8123265
$385.00
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for NPHP3 antibody (AA 1092-1142) (ABIN8123265)

Target

See all NPHP3 Antibodies
NPHP3 (Nephronophthisis 3 (Adolescent) (NPHP3))

Reactivity

Human, Mouse

Host

  • 16
  • 1
Rabbit

Clonality

  • 16
  • 1
Polyclonal

Conjugate

  • 12
  • 1
  • 1
  • 1
  • 1
  • 1
This NPHP3 antibody is un-conjugated

Application

  • 16
  • 12
  • 10
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 3
    • 3
    • 2
    • 1
    • 1
    AA 1092-1142

    Purpose

    NPHP3 Antibody

    Specificity

    This antibody detects endogenous levels of NPHP3 at Human/Mouse

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogen

    Synthesized peptide derived from human NPHP3 AA range: 1092-1142

    Isotype

    IgG
  • Application Notes

    WB 1:500-2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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

    -20 °C

    Storage Comment

    Store at -20°C/1 year

    Expiry Date

    12 months
  • Target

    NPHP3 (Nephronophthisis 3 (Adolescent) (NPHP3))

    Alternative Name

    NPHP3

    Background

    Background: This gene encodes a protein containing a coiled-coil (CC) domain, a tubulin-tyrosine ligase (TTL) domain, and a tetratrico peptide repeat (TPR) domain. The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development. Mutations in this gene are associated with nephronophthisis type 3, and also with renal-hepatic-pancreatic dysplasia, and Meckel syndrome type 7. Naturally occurring read-through transcripts exist between this gene and the downstream ACAD11 (acyl-CoA dehydrogenase family, member 11) gene. [provided by RefSeq, Feb 2011],

    Gene Name: NPHP3 KIAA2000

    Protein Name: NPHP3

    Gene ID

    27031

    UniProt

    Q7Z494

    Pathways

    cAMP Metabolic Process
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