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CDMP1 Antibody

CDMP1 Antibody size: 0.1ml 263

Supplier BIOSS PRIMARY UNCONJUGATED ANTIBODIES
Price 263
Size 0.1ml
Contact us Ask Component cell markers and DNA bp. markers are genetic markerser genes or DNA sequenceswith selection audit
Long nameCDMP1 Primary Polyclonal Antibody
Also known asCDMP1 PAb
CategoryPrimary Antibodies
ConjugationUnconjugated
Target AntigenCDMP1
SpecificityThis is a highly specific antibody against CDMP1
Modification(s)None
Modification site(s)Unmodified antibody
ClonalityPolyclonal antibody
Clone numberPolyclonal antibody
Concentration1ug per 1ul
SourceThis antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human CDMP1/GDF5
Gene ID number8200
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 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 methodThis 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 CDMP-1, CDMP1, Cartilage-derived morphogenetic protein 1, GDF-5, GDF5_HUMAN, Gdf 5, Growth dferentiation factor 5, Growth/dferentiation factor 5, LAP4, Radotermin, Cartilage derived morphogenetic protein 1
PropertiesC, 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 targetCDMP1
Short nameCDMP1 Antibody
Technique antibodies against human proteins, antibodies for, Antibody
Alternative nameCDMP1 (Antibody to)
Alternative techniqueantibodies
Identity 4220
Gene GDF5
Long gene name growth differentiation factor 5
Synonyms CDMP1 BMP14
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

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