Name : Anti-CABC1 (Polyclonal), ALEXA Fluor 594
Supplier : BIOSS POLYCLONAL ANTIBODIES
Price :489
SKU : GEN2565180841
| Type | Conjugated Primary Antibody |
| Conjugated with | 594, ALEXA FLUOR® |
| Host organism | Rabbit (Oryctolagus cuniculus) |
| Target Protein/Peptide | CABC1 |
| Specificity | This antibody reacts specifically with CABC1 |
| Modification | No modification has been applied to this antibody |
| Modification site | None |
| Clonality | Polyclonal Antibody |
| Clone | Polyclonal Antibodies |
| Concentration | 1ug per 1ul |
| Subcellular locations | N/A |
| Antigen Source | KLH conjugated synthetic peptide derived from human ADCK3/CABC1 |
| Gene ID | N/A |
| Swiss Prot | N/A |
| Applications | IF(IHC-P) |
| Applications with corresponding dilutions | IF(IHC-P)(1:50-200) |
| Cross reactive species | Mouse (Mus musculus), Rat (Rattus norvegicus), Human (Homo sapiens) |
| Cross Reactive Species details | However, note that due to limited knowledge it is impossible to predict with 100% guarantee that the antibody does not corss react with any other species, No significant cross reactivity has been observed for this antibody for the tested species |
| Background information | CoQ10 deficiency is an autosomal recessive disorder with variable manifestations, It can be associated with three main clinical phenotypes: a predominantly myopathic form with central nervous system involvement, Patients can manifest brisk tendon reflexes and Hoffmann sign, Patients show progressive incoordination of gait and often poor coordination of hands, SCAR9 is an autosomal recessive form characterized by gait ataxia and cerebellar atrophy with slow progression and few associated features, Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders, also known as autosomal recessive cerebellar ataxia type 2 (ARCA2), an infantile encephalomyopathy with renal dysfunction and an ataxic form with cerebellar atrophy, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord, exercise intolerance and elevated serum lactate, mild axonal degeneration of the sural nerve, mild psychomotor retardation, speech and eye movements, Defects in ADCK3 are the cause of spinocerebellar ataxia autosomal recessive type 9 (SCAR9) [MIM:612016], Involvement in disease:Defects in ADCK3 are a cause of coenzyme Q10 deficiency (CoQ10 deficiency), May be a chaperone-like protein essential for the proper conformation and functioning of protein complexes in the respiratory chain, Tissue specificity:Ubiquitously expressed with a relatively greater abundance in heart and skeletal muscle |
| Purification method | Purified by Protein A |
| Storage | 50% glycerol and 0, Store at 4°, 09% sodium azide, C for 12 months, Water buffered solution containing 100ug/ml BSA |
| Excitation emission | 590nm/617nm |
| Synonyms | COQ8 SCAR9 |
| Also known as | CABC1 Polyclonal Antibody |
| Other name | Anti-CABC1 Polyclonal |
| Advisory | For antibodies that are in liquid form or reconstituted lyophilized antibodies small amounts could become entrapped on the seal or the walls of the tube, Prior to use briefly centrifuge the vial to gather all the solution on the bottom, specificity and sensitivity, thus reducing its reactivity, Avoid freeze/thaw cycles as they may denaturate the polypeptide chains of the antibody |
| Properties | For facs or microscopy Alexa 1 conjugate |
| Conjugation | Alexa Fluor |
| Group | Polyclonals and antibodies |
| About | The advantage is that there are more epitopes available in a polyclonal antiserum to detect the proteins than in monoclonal sera, immunohistochemistry on frozen slices or parrafin fixed tissues, Polyclonals can be used for Western blot |
| Gene target | CABC1 |
| Short name | Anti-CABC1 (Polyclonal) Fluor 594 |
| Technique | Pabs are a collection of immunoglobulin , Polyclonal antibodies , each identifying a different , whereas , (pAbs) are mostly rabbit or goat , B cells, Polyclonal, antibodies , antigen, come from a single N cell lineage, epitope, molecules that react against a specific , monoclonal antibodies , that are secreted by different  |
| Label | ALEXA |
| Alternative name | ALEXA Fluor 594, antibody to-CABC1 (polyclonal) |
| Alternative technique | polyclonals |
| Identity | 16812 |
| Gene | COQ8A |
| Long gene name | coenzyme Q8A |
| Synonyms gene | CABC1 ADCK3 |
| Synonyms gene name | ABC1 activity of bc1 complex homolog (S, ABC1 activity of bc1 complex like (S, S, chaperone-ABC1 (activity of bc1 complex, pombe) aarF domain containing kinase 3 , pombe) chaperone, pombe)-like chaperone |
| Synonyms name | coenzyme Q8 homolog (yeast) |
| Locus | 1q42, 13 |
| Discovery year | 2001-10-31 |
| GenBank acession | AJ278126 |
| Entrez gene record | 56997 |
| Pubmed identfication | 18319072 18319074 25498144 |
| RefSeq identity | NM_020247 |
| Havana BLAST/BLAT | OTTHUMG00000037621 |
| Locus Specific Databases | LRG_1092 |