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B9D1 antibody (AA 1-130)

This Rabbit Polyclonal antibody specifically detects B9D1 in IHC, WB and IF. It exhibits reactivity toward Human.
Catalog No. ABIN6137409

Quick Overview for B9D1 antibody (AA 1-130) (ABIN6137409)

Target

See all B9D1 Antibodies
B9D1 (B9 Protein Domain 1 (B9D1))

Reactivity

  • 10
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 9
  • 1
Rabbit

Clonality

  • 10
Polyclonal

Conjugate

  • 10
This B9D1 antibody is un-conjugated

Application

  • 9
  • 6
  • 4
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 3
    • 3
    • 1
    • 1
    • 1
    AA 1-130

    Sequence

    MATASPSVFL LMVNGQVESA QFPEYDDLYC KYCFVYGQDW APTAGLEEGI SQITSKSQDV RQALVWNFPI DVTFKSTNPY GWPQIVLSVY GPDVFGNDVV RGYGAVHVPF SPGRHKRTIP MFVPESTSKL

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-130 of human B9D1 (NP_056496.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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. Avoid freeze / thaw cycles.
  • Target

    B9D1 (B9 Protein Domain 1 (B9D1))

    Alternative Name

    B9D1

    Background

    This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17.,B9D1,B9,EPPB9,JBTS27,MKS9,MKSR1,Cell Biology & Developmental Biology,Cell Cycle,Centrosome,B9D1

    Molecular Weight

    16 kDa/22 kDa

    Gene ID

    27077

    UniProt

    Q9UPM9
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