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SCNM1 antibody

The Rabbit Polyclonal anti-SCNM1 antibody has been validated for ELISA and WB. It is suitable to detect SCNM1 in samples from Human.
Catalog No. ABIN7231288

Quick Overview for SCNM1 antibody (ABIN7231288)

Target

See all SCNM1 Antibodies
SCNM1 (Sodium Channel Modifier 1 (SCNM1))

Reactivity

  • 15
  • 5
  • 4
  • 1
  • 1
Human

Host

  • 13
  • 2
Rabbit

Clonality

  • 13
  • 2
Polyclonal

Conjugate

  • 11
  • 2
  • 1
  • 1
This SCNM1 antibody is un-conjugated

Application

  • 11
  • 9
  • 4
  • 1
ELISA, Western Blotting (WB)
  • Purpose

    SCNM1 Polyclonal Antibody

    Specificity

    The antibody detects endogenous levels of SCNM1 protein

    Purification

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    Immunogen

    Synthesized peptide derived from part region of human SCNM1 protein

    Isotype

    IgG
  • Application Notes

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    Comment

    Primary Antibody

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • Target

    SCNM1 (Sodium Channel Modifier 1 (SCNM1))

    Alternative Name

    SCNM1

    Background

    Rabbit Anti-SCNM1 Polyclonal Antibody,Sodium channel modifier 1,SCNM1 is a zinc finger protein and putative splicing factor. In mice, Scnm1 modifies phenotypic expression of Scn8a mutations. Diseases associated with SCNM1 include Lennox-Gastaut Syndrome. GO annotations related to this gene include enzyme binding. Plays a role in RNA splicing, possibly contributing to the recognition of non-consensus donor sites.,SCNM1

    Molecular Weight

    observerd band 25kDa

    Gene ID

    79005

    UniProt

    Q9BWG6
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