Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

TMEM43 antibody (AA 80-310)

This Rabbit Polyclonal antibody specifically detects TMEM43 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN6149266

Quick Overview for TMEM43 antibody (AA 80-310) (ABIN6149266)

Target

See all TMEM43 Antibodies
TMEM43 (Transmembrane Protein 43 (TMEM43))

Reactivity

  • 19
  • 3
  • 1
Human

Host

  • 19
Rabbit

Clonality

  • 17
  • 2
Polyclonal

Conjugate

  • 10
  • 3
  • 2
  • 2
  • 1
  • 1
This TMEM43 antibody is un-conjugated

Application

  • 14
  • 14
  • 13
  • 2
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 7
    • 1
    • 1
    • 1
    • 1
    AA 80-310

    Sequence

    VAPENEGRLV HIIGALRTSK LLSDPNYGVH LPAVKLRRHV EMYQWVETEE SREYTEDGQV KKETRYSYNT EWRSEIINSK NFDREIGHKN PSAMAVESFM ATAPFVQIGR FFLSSGLIDK VDNFKSLSLS KLEDPHVDII RRGDFFYHSE NPKYPEVGDL RVSFSYAGLS GDDPDLGPAH VVTVIARQRG DQLVPFSTKS GDTLLLLHHG DFSAEEVFHR ELRSNSMKTW G

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 80-310 of human TMEM43 (NP_077310.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    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

    TMEM43 (Transmembrane Protein 43 (TMEM43))

    Alternative Name

    TMEM43

    Background

    This gene belongs to the TMEM43 family. Defects in this gene are the cause of familial arrhythmogenic right ventricular dysplasia type 5 (ARVD5), also known as arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5). Arrhythmogenic right ventricular dysplasia is an inherited disorder, often involving both ventricles, and is characterized by ventricular tachycardia, heart failure, sudden cardiac death, and fibrofatty replacement of cardiomyocytes. This gene contains a response element for PPAR gamma (an adipogenic transcription factor), which may explain the fibrofatty replacement of the myocardium, a characteristic pathological finding in ARVC.,TMEM43,ARVC5,ARVD5,EDMD7,LUMA,Signal Transduction,TMEM43

    Molecular Weight

    44 kDa

    Gene ID

    79188

    UniProt

    Q9BTV4
You are here:
Chat with us!