| Long name: |
FAHD1 Primary Polyclonal Antibody |
| Also known as: |
FAHD1 PAb |
| Category: |
Primary Antibodies |
| Conjugation: |
Unconjugated |
| Target Antigen: |
FAHD1 |
| Specificity: |
This is a highly specific antibody against FAHD1 |
| 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 FAHD1 |
| Gene ID number: |
81889 |
| 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, Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors, Present as a homodimer, Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias, The GAN gene is located on chromosome 16 and, The gene that encodes FAHD1 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, making up nearly 3% of human cellular DNA, may lead to giant axonal neuropathy, though through the CREBBP gene which encodes a critical CREB binding protein, which encodes over 900 genes in approximately 90 million base pairs, with mutation, FAHD1 is a 224 amino acid protein belonging to the FAH family |
| 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: |
C16orf36, Chromosome 16 open reading frame 36, DKFZP566J2046, FAHD1, FAHD1_HUMAN, Fumarylacetoacetate hydrolase domain containing protein 1, Fumarylacetoacetate hydrolase domain-containing protein 1, MGC74876, YISK like, YISK like/RJD15, YISKL, YisK-like protein, mitochondrial, Acylpyruvase FAHD1 |
| 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: |
FAHD1 |
| Short name: |
FAHD1 Antibody |
| Technique: |
antibodies against human proteins, antibodies for, Antibody |
| Alternative name: |
FAHD1 (Antibody to) |
| Alternative technique: |
antibodies |
| Identity: |
14169 |
| Gene: |
FAHD1 |
More about : FAHD1 |
| Long gene name: |
fumarylacetoacetate hydrolase domain containing 1 |
| Synonyms gene: |
C16orf36 |
| Synonyms gene name: |
chromosome 16 open reading frame 36 |
| Synonyms: |
DKFZP566J2046 |
| Synonyms name: |
acylpyruvate hydrolase |
| Locus: |
16p13, 3 |
| Discovery year: |
2000-12-21 |
| GenBank acession: |
BC063017 |
| Entrez gene record: |
81889 |
| Pubmed identfication: |
21878618 |
| RefSeq identity: |
NM_001018104 |
| Havana BLAST/BLAT: |
OTTHUMG00000128663 |