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ALX1 antibody (AA 97-122)

This Rabbit Polyclonal antibody specifically detects ALX1 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN1538707

Quick Overview for ALX1 antibody (AA 97-122) (ABIN1538707)

Target

See all ALX1 Antibodies
ALX1 (ALX Homeobox 1 (ALX1))

Reactivity

  • 35
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 31
  • 4
Rabbit

Clonality

  • 31
  • 4
Polyclonal

Conjugate

  • 12
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ALX1 antibody is un-conjugated

Application

  • 19
  • 14
  • 13
  • 13
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB37559
  • Binding Specificity

    • 15
    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 97-122

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This ALX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 97-122 amino acids from the Central region of human ALX1.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

    Storage Comment

    ALX1 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • Target

    ALX1 (ALX Homeobox 1 (ALX1))

    Alternative Name

    ALX1

    Background

    The specific function of this gene has yet to be determined in humans, however, in rodents, it is necessary for survival of the forebrain mesenchyme and may also be involved in development of the cervix. Mutations in the mouse gene lead to neural tube defects such as acrania and meroanencephaly. [provided by RefSeq].

    Molecular Weight

    36961

    Gene ID

    8092

    NCBI Accession

    NP_008913

    UniProt

    Q15699

    Pathways

    Tube Formation
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