DYM Antibody
Product Specifications
Background
This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia, which involve both skeletal defects and mental retardation.
NCBI Gene ID
54808
Swiss Prot
Q7RTS9
Host
Rabbit
Reactivity
Human
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-250 of human DYM (NP_060123.3) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Other
Purification
Affinity purification
Positive Control
293T
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=23-467
Calculated Molecular Weight
Observed: 78kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
DYM
Positive Control 2
HepG2
Positive Control 3
HeLa
NCBI Official Name
Dymeclin
NCBI Organism
Homo sapiens
Other Product Names
DMC, SMC, dymeclin, dyggve-Melchior-Clausen syndrome protein
Tested Applications
WB
Physical Properties
Liquid
Curated Selection
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