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Anti-SAMD7 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Anti-SAMD7 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Catalog #: 10665-232
Supplier:  Bioss
Anti-SAMD7 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Catalog #: 10665-232
Supplier:  Bioss
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Specifications

  • Antibody type:
    Primary
  • Antigen name:
    Sterile Alpha Motif Domain Containing 7
  • Clonality:
    Polyclonal
  • Gene ID:
    344658
  • Host:
    Rabbit
  • Isotype:
    IgG
  • Reactivity:
    Human,
    Rat,
    Mouse
  • Antigen symbol:
    SAMD7
  • Conjugation:
    Alexa Fluor® 647
  • ImmunoChemistry:
    Yes
  • Size:
    100 µL
  • Cross adsorption:
    No
  • Form:
    liquid
  • Antigen synonyms:
    Sterile alpha mot domain-containing protein 7.|Samd 7|sterile alpha mot domain containing 7|SAMD7_HUMAN|Samd7|SAM domain-containing protein 7|Samd-7
  • Storage buffer:
    Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% sodium azide. Store at 4°C for 12 months.
  • Storage temperature:
    Store at –20 °C for 12 months
  • Concentration:
    1 μg/μl
  • Shipping temperature:
    4°C
  • Purification:
    Purified by Protein A
  • Cat. no.:
    10665-232
  • Supplier No.:
    BS-9003R-A647

Specifications

About this item

The sterile alpha motif (SAM) domain is a 70 residue structure found in a large number of proteins involved in diverse processes present throughout the eukaryotes. The SAM domain is known to bind RNA and is arranged in a small five-helix bundle with two large interfaces. SAMD7 (Sterile alpha motif domain-containing protein 7), is a 446 amino acid protein encoded by the SAMD7 gene which maps to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

Recommended Dilutions: IF(IHC-P): 1:50-200

Type: Primary
Antigen: SAMD7
Clonality: Polyclonal
Clone:
Conjugation: Alexa Fluor® 647
Epitope:
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat

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