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TMEM67 antibody (AA 780-940)

The Rabbit Polyclonal anti-TMEM67 antibody has been validated for WB. It is suitable to detect TMEM67 in samples from Human.
Catalog No. ABIN7270970

Quick Overview for TMEM67 antibody (AA 780-940) (ABIN7270970)

Target

See all TMEM67 Antibodies
TMEM67 (Transmembrane Protein 67 (TMEM67))

Reactivity

  • 20
  • 4
  • 2
Human

Host

  • 21
Rabbit

Clonality

  • 20
  • 1
Polyclonal

Conjugate

  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TMEM67 antibody is un-conjugated

Application

  • 9
  • 6
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 780-940

    Purpose

    TMEM67 Rabbit pAb

    Sequence

    LSHKCFGYYI HGRSVHGHAD TNMEEMNMNL KREAENLCSQ RGLVPNTDGQ TFEIAISNQM RQHYDRIHET LIRKNGPARL LSSSASTFEQ SIKAYHMMNK FLGSFIDHVH KEMDYFIKDK LLLERILGME FMEPMEKSIF YNDEGYSFSS VLYYGNEATL L

    Cross-Reactivity

    Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 780-940 of human TMEM67 (NP_714915.3).

    Isotype

    IgG
  • Application Notes

    WB,1:200 - 1:2000

    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

    TMEM67 (Transmembrane Protein 67 (TMEM67))

    Alternative Name

    TMEM67

    Background

    The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).,TMEM67,JBTS6,MECKELIN,MKS3,NPHP11,TNEM67,meckelin,TMEM67

    Molecular Weight

    103kDa/111kDa

    Gene ID

    91147

    UniProt

    Q5HYA8
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