Name : Anti-CDMP1 (Polyclonal), ALEXA Fluor 594
Supplier : BIOSS POLYCLONAL ANTIBODIES
Price :489
SKU : GEN7240126064
| Type | Conjugated Primary Antibody |
| Conjugated with | 594, ALEXA FLUOR® |
| Host organism | Rabbit (Oryctolagus cuniculus) |
| Target Protein/Peptide | CDMP1 |
| Specificity | This antibody reacts specifically with CDMP1 |
| 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 CDMP1/GDF5 |
| Gene ID | 8200 |
| 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 | AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet, AMDH is an autosomal recessive form of dwarfism, AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet, Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes, Patients have limb abnormalities, The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers), and hand/foot malformations, very short limbs, with the middle and distal segments being most affected and the lower limbs more affected than the upper, Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) , Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH), Defects in GDF5 are the cause of brachydactyly type C (BDC) |
| 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 | CDMP1 BMP14 |
| Also known as | CDMP1 Polyclonal Antibody |
| Other name | Anti-CDMP1 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 | CDMP1 |
| Short name | Anti-CDMP1 (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-CDMP1 (polyclonal) |
| Alternative technique | polyclonals |
| Identity | 4220 |
| Gene | GDF5 |
| Long gene name | growth differentiation factor 5 |
| Synonyms name | cartilage-derived morphogenetic protein-1 |
| Locus | 20q11, 22 |
| Discovery year | 1997-12-05 |
| GenBank acession | X80915 |
| Entrez gene record | 8200 |
| Pubmed identfication | 9288091 9288098 |
| Havana BLAST/BLAT | OTTHUMG00000032341 |