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Rabbit Anti-MAMDC2 antibody
Rabbit Anti-MAMDC2 antibody
MAM domain-containing protein 2; MAM domain-containing proteoglycan; MAMC2_HUMAN; Mamcan; Mamdc2.
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  • NO.:SL18641R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Dog,Pig,Cow,Horse,Sheep,)
    Applications:ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Product Name MAMDC2
Chinese Name MAMDC2蛋白抗体
Alias MAM domain-containing protein 2; MAM domain-containing proteoglycan; MAMC2_HUMAN; Mamcan; Mamdc2.  
Research Area Cell biology  Developmental biology  Signal transduction  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Sheep, )
Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 75kDa
Cellular localization Extracellular matrix Secretory protein 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human MAMDC2: 601-686/686 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail MAMDC2 is a 686 amino acid secreted protein that localizes to extracellular matrix. Containing four MAM domains and existing as two alternatively spliced isoforms, MAMDC2 is encoded by a gene located on human chromosome 9q21.11. Chromosome 9 consists of about 145 million bases, 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, Familial dysautonomia and certain leukemias are also associated with chromosome 9.

Subcellular Location:
Secreted > extracellular space > extracellular matrix.

Post-translational modifications:
O-glycosylated.

Similarity:
Contains 4 MAM domains.

SWISS:
Q7Z304

Gene ID:
256691

Database links:

Entrez Gene: 256691 Human

Omim: 612879 Human

SwissProt: Q7Z304 Human

Unigene: 547172 Human



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