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Rabbit Anti-FLYWCH1 antibody
Rabbit Anti-FLYWCH1 antibody
DKFZp761A132; FWCH1_HUMAN; FLYWCH type zinc finger containing protein 1; FLYWCH zinc finger 1; FLYWCH-type zinc finger 1; KIAA1552.
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Details

Product Name FLYWCH1
Chinese Name FLYWCH1蛋白抗体
Alias DKFZp761A132; FWCH1_HUMAN; FLYWCH type zinc finger containing protein 1; FLYWCH zinc finger 1; FLYWCH-type zinc finger 1; KIAA1552.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, )
Applications IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 90kDa
Cellular localization The nucleus 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FLYWCH1: 631-715/715 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail FLYWCH1 (FLYWCH-type zinc finger 1) is a 716 amino acid nuclear protein containing five FLYWCH-type zinc fingers. Existing as five alternatively spliced isoforms, FLYWCH1 is encoded by a gene located on human chromosome 16p13.3. Chromosome 16 encodes over 900 genes and comprises nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene, which encodes a critical CREB binding protein. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

Function:
FLYWCH, also commonly known as FLYWCH-type zinc finger 1, is a nuclear DNA-binding protein. It contains 5 FLYWCH-type zinc finger domains and is 716 amino acids in length. There are five isoforms of the protein produced by alternative splicing. Isoform 1 (80 kDa) is the canonical form.

Subcellular Location:
Nuclear

Similarity:
ontains 5 FLYWCH-type zinc fingers.

SWISS:
Q4VC44

Gene ID:
84256

Database links:

Entrez Gene: 84256 Human

SwissProt: Q4VC44 Human



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