Home > Product > Antibody > Rabbit Anti-RNF10/FITC Conjugated antibody
RING finger protein 10; RNF10; RNF10_HUMAN.
Cat:
SL9175R-FITC
Species Reactivity:
(predicted: Human,Mouse,Rat,Chicken,Pig,Cow,Sheep,)
Immunogen:
KLH conjugated synthetic peptide derived from human RNF10
Format:
Lyophilized or Liquid
Storage instructions:
Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of ant
Buffer:
0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
IF=1:50-200not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
Calculated MW:
90kDa
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Unit:
Price: $
Product PDFs
Datasheet:


background:
The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF10 (ring finger protein 10), also known as RIE2, is an 811 amino acid protein that localizes to the cytoplasm and contains one RING-type zinc finger. Existing as multiple alternatively spliced isoforms, RNF10 interacts with MOX-2 and is thought to regulate its transcription in schwann cells, possibly playing a role in myelin formation. The gene encoding RNF10 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.

Function:
Transcriptional factor involved in the regulation of MAG expression. Participates in the peripheral nerve development and Schawnn cell differentiation (By similarity).

Subunit:
Interacts with MEOX2.

Subcellular Location:
Cytoplasmic and Nuclear

Similarity:
Belongs to the RNF10 family.
Contains 1 RING-type zinc finger.

Database links:

Entrez Gene: 9921 Human

Entrez Gene: 50849 Mouse

Entrez Gene: 288710 Rat

SwissProt: Q8N5U6 Human

SwissProt: Q3UIW5 Mouse

SwissProt: Q5XI59 Rat

Unigene: 442798 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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