| Long name: |
FOPNL/C16orf63 Primary Polyclonal Antibody |
| Also known as: |
FOPNL/C16orf63 PAb |
| Category: |
Primary Antibodies |
| Conjugation: |
Unconjugated |
| Target Antigen: |
FOPNL/C16orf63 |
| Specificity: |
This is a highly specific antibody against FOPNL/C16orf63 |
| Modification(s): |
None |
| Modification site(s): |
Unmodified antibody |
| Clonality: |
Polyclonal antibody |
| Clone number: |
Polyclonal antibody |
| Concentration: |
1ug per 1ul |
| Source: |
This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human FOPNL/C16orf63 |
| Gene ID number: |
123811 |
| Tested Applications: |
IF(IHC-P), IHC-P, WB |
| Recommended dilutions: |
IF(IHC-P)(1:50-200), IHC-P(1:100-500), WB(1:100-1000) |
| Cross reactivity: |
Mouse, Rat, Human |
| Cross reactive species details: |
not every possible cross-reactivity is known, Due to limited amount of testing and knowledge |
| Background of the target antigen: |
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, Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene, Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias, The C16orf63 gene product has been provisionally designated C16orf63 pending further characterization, The GAN gene is located on chromosome 16 and, The gene that encodes C16orf63 maps to human chromosome 16, The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, a nervous system disorder characterized by increasing malfunction with growth, also known as FLJ31153 or DKFZp686N1651, is a 174 amino acid protein that contains one LisH domain, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders, may lead to giant axonal neuropathy, though through the CREBBP gene which encodes a critical CREB binding protein, with mutation, C16orf63 |
| Purification method: |
This antibody was purified via Protein A |
| Storage conditions: |
50% glycerol and 0, Store at -20°, 09% sodium azide, C for up to 1 year, Keep the antibody in aqueous buffered solution containing 1% BSA |
| Synonym names: |
FGFR1OP N terminal like, FGFR1OP N-terminal-like protein, FOP-related protein of 20 kDa, FOPNL_HUMAN, FOR20, Fopnl, LisH domain containing protein C16orf63, LisH domain-containing protein FOPNL, PHSECRG2, Pluripotent embryonic stem cell related protein, C16orf63 |
| Properties: |
C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Unconjugated Antibodies they should be stored frozen at - 24° |
| Gene target: |
FOPNL/C16orf63 |
| Short name: |
FOPNL/C16orf63 Antibody |
| Technique: |
antibodies against human proteins, antibodies for, Antibody |
| Alternative name: |
FOPNL/C16orf63 (Antibody to) |
| Alternative technique: |
antibodies |
| Identity: |
26435 |
| Gene: |
FOPNL |
More about : FOPNL |
| Long gene name: |
FGFR1OP N-terminal like |
| Synonyms gene: |
C16orf63 |
| Synonyms gene name: |
chromosome 16 open reading frame 63 |
| Synonyms: |
DKFZp686N1651 FLJ31153 PHSECRG2 FOR20 |
| Synonyms name: |
pluripotent embryonic stem cell-related protein FOP-related protein of 20 kDa |
| Locus: |
16p13, 11 |
| Discovery year: |
2006-02-20 |
| GenBank acession: |
AL832498 |
| Entrez gene record: |
123811 |
| Pubmed identfication: |
20551181 |
| RefSeq identity: |
NM_144600 |
| Havana BLAST/BLAT: |
OTTHUMG00000129923 |