Naegleria gruberi Schardinger-质粒载体-ATCC-DSM-CCUG-泰斯拓生物

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Naegleria gruberi Schardinger
Naegleria gruberi Schardinger
规格:
货期:
编号:TS156293
品牌:Testobio
产品名称: Naegleria gruberi Schardinger
商品货号: TS156293
Strain Designations: NEG-M
Biosafety Level: 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Isolation: Derived in 1969 from strain NEG (See ATCC® 30223™)
Product Format: frozen
Storage Conditions: Frozen Cultures:
-70°C for 1 week; liquid N2 vapor for long term storage

Freeze-dried Cultures:
2-8°C

Live Cultures:
See Protocols section for handling information
Type Strain: no
Comments:
Chemically defined medium
Circular ribosomal RNA genes
rRNA Genes on 14-Kilobase- Pair Plasmid
Cell differentiation
Freeze preservation of pathogenic and nonpathogenic species
Medium: ATCC® Medium 1034: Modified PYNFH medium (Available from ATCC as ATCC cat. no. 327-X)
ATCC® Medium 710: Nelsons Culture Medium For Naegleria
ATCC® Medium 803: M7 medium
ATCC® Medium 902: Schusters axenic Naegleria medium
Growth Conditions:
Temperature: 25°C
Culture System: Axenic
Cryopreservation: Harvest and Preservation
  1. Harvest cells from a culture that is at or near peak density by centrifugation at 600 x g for 5 min. Pool the cell pellets into a single tube.
  2. Adjust the concentration of cells to 2.0 x 106/mL.xa0 If the concentration is too low, centrifuge at 600 x g for 5 minutes and resuspend the cell pellet with a volume of supernatant to yield the desired concentration.
  3. Prepare a 15% (v/v) sterile DMSO solution in ATCC medium 1034 as follows:
    1. Add the required volume of DMSO to a glass screw-capped test tube and place on ice.xa0 Allow the DMSO to solidify.
    2. Add the required volume of refrigerated ATCC medium 1034.xa0 Dissolve the DMSO by inverting several times.xa0 If the DMSO solution is not prepared on ice, an exothermic reaction will occur that may precipitate certain components of the medium.
  4. Mix the cell preparation and the DMSO in equal portions. Thus, the final concentration will be 106 and 7.5% (v/v) DMSO. The time from the mixing of the cell preparation and DMSO stock solution to the start of the freezing process should be no less than 15 min and no longer than 60 min.
  5. Dispense in 0.5 mL aliquots into 1.0 mL toxa02.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation).
  6. Place vials in a controlled rate freezing unit. From room temperature cool at -1°C/min to -40°C. If freezing unit can compensate for the heat of fusion, maintain rate at -1°C/min through heat of fusion. At -40°C plunge ampules into liquid nitrogen.
  7. The frozen preparations are stored in either the vapor or liquid phase of a nitrogen refrigerator.
  8. To establish a culture from the frozen state place an ampule in a water bath set at 35°C. Immerse the vial just sufficiently to cover only the frozen material. Do not agitate the vial.
  9. Immediately after thawing, do not leave in the water bath, aseptically remove the contents of the ampule and inoculate into a fresh tube or flask of ATCC medium 1034.
  10. Incubate at 25°C with the cap screwed on tightly (incubate a test tube on a 15° horizontal slant).
Name of Depositor: C Fulton
References:

Clark CG, Cross GA. Circular ribosomal RNA genes are a general feature of schizopyrenid amoebae. J. Protozool. 35: 326-329, 1988. PubMed: 2840492

Clark CG, Cross GA. rRNA genes of Naegleria gruberi are carried exclusively on a 14- kilobase-pair plasmid. Mol. Cell. Biol. 7: 3027-3031, 1987. PubMed: 2823115

De Jonckheere JF. A century of research on the amoeboflagellate genus Naegleria. Acta Protozool. 41: 309-342, 2002.

Fulton C. Cell differentiation in Naegleria gruberi. Annu. Rev. Microbiol. 31: 597-629, 1977. PubMed: 334046

Fulton C, et al. Chemically defined media for cultivation of Naegleria gruberi. Proc. Natl. Acad. Sci. USA 81: 2406-2410, 1984.

Fulton C. Methods in cell physiology. vol. 4New York: Academic Press; 1970.

Simione FP Jr., Daggett PM. Freeze preservation of pathogenic and nonpathogenic Naegleria species. J. Parasitol. 62: 49, 1976. PubMed: 1255382

Simpson AGB, et al. The evolutionary history of kinetoplastids and their kinetoplasts. Mol. Biol. Evol. 19: 2071-2083, 2002. PubMed: 12446799

Cross References:

Nucleotide (GenBank) : M18732 N.gruberi 18S subunit ribosomal RNA gene.

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Naegleria gruberi Schardinger

  • 货号: TS156293
  • 好评
有货
  • 品牌 : TESTOBIO
产品名称: Naegleria gruberi Schardinger
商品货号: TS156293
Strain Designations: NEG-M
Biosafety Level: 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Isolation: Derived in 1969 from strain NEG (See ATCC® 30223™)
Product Format: frozen
Storage Conditions: Frozen Cultures:
-70°C for 1 week; liquid N2 vapor for long term storage

Freeze-dried Cultures:
2-8°C

Live Cultures:
See Protocols section for handling information
Type Strain: no
Comments:
Chemically defined medium
Circular ribosomal RNA genes
rRNA Genes on 14-Kilobase- Pair Plasmid
Cell differentiation
Freeze preservation of pathogenic and nonpathogenic species
Medium: ATCC® Medium 1034: Modified PYNFH medium (Available from ATCC as ATCC cat. no. 327-X)
ATCC® Medium 710: Nelsons Culture Medium For Naegleria
ATCC® Medium 803: M7 medium
ATCC® Medium 902: Schusters axenic Naegleria medium
Growth Conditions:
Temperature: 25°C
Culture System: Axenic
Cryopreservation: Harvest and Preservation
  1. Harvest cells from a culture that is at or near peak density by centrifugation at 600 x g for 5 min. Pool the cell pellets into a single tube.
  2. Adjust the concentration of cells to 2.0 x 106/mL.xa0 If the concentration is too low, centrifuge at 600 x g for 5 minutes and resuspend the cell pellet with a volume of supernatant to yield the desired concentration.
  3. Prepare a 15% (v/v) sterile DMSO solution in ATCC medium 1034 as follows:
    1. Add the required volume of DMSO to a glass screw-capped test tube and place on ice.xa0 Allow the DMSO to solidify.
    2. Add the required volume of refrigerated ATCC medium 1034.xa0 Dissolve the DMSO by inverting several times.xa0 If the DMSO solution is not prepared on ice, an exothermic reaction will occur that may precipitate certain components of the medium.
  4. Mix the cell preparation and the DMSO in equal portions. Thus, the final concentration will be 106 and 7.5% (v/v) DMSO. The time from the mixing of the cell preparation and DMSO stock solution to the start of the freezing process should be no less than 15 min and no longer than 60 min.
  5. Dispense in 0.5 mL aliquots into 1.0 mL toxa02.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation).
  6. Place vials in a controlled rate freezing unit. From room temperature cool at -1°C/min to -40°C. If freezing unit can compensate for the heat of fusion, maintain rate at -1°C/min through heat of fusion. At -40°C plunge ampules into liquid nitrogen.
  7. The frozen preparations are stored in either the vapor or liquid phase of a nitrogen refrigerator.
  8. To establish a culture from the frozen state place an ampule in a water bath set at 35°C. Immerse the vial just sufficiently to cover only the frozen material. Do not agitate the vial.
  9. Immediately after thawing, do not leave in the water bath, aseptically remove the contents of the ampule and inoculate into a fresh tube or flask of ATCC medium 1034.
  10. Incubate at 25°C with the cap screwed on tightly (incubate a test tube on a 15° horizontal slant).
Name of Depositor: C Fulton
References:

Clark CG, Cross GA. Circular ribosomal RNA genes are a general feature of schizopyrenid amoebae. J. Protozool. 35: 326-329, 1988. PubMed: 2840492

Clark CG, Cross GA. rRNA genes of Naegleria gruberi are carried exclusively on a 14- kilobase-pair plasmid. Mol. Cell. Biol. 7: 3027-3031, 1987. PubMed: 2823115

De Jonckheere JF. A century of research on the amoeboflagellate genus Naegleria. Acta Protozool. 41: 309-342, 2002.

Fulton C. Cell differentiation in Naegleria gruberi. Annu. Rev. Microbiol. 31: 597-629, 1977. PubMed: 334046

Fulton C, et al. Chemically defined media for cultivation of Naegleria gruberi. Proc. Natl. Acad. Sci. USA 81: 2406-2410, 1984.

Fulton C. Methods in cell physiology. vol. 4New York: Academic Press; 1970.

Simione FP Jr., Daggett PM. Freeze preservation of pathogenic and nonpathogenic Naegleria species. J. Parasitol. 62: 49, 1976. PubMed: 1255382

Simpson AGB, et al. The evolutionary history of kinetoplastids and their kinetoplasts. Mol. Biol. Evol. 19: 2071-2083, 2002. PubMed: 12446799

Cross References:

Nucleotide (GenBank) : M18732 N.gruberi 18S subunit ribosomal RNA gene.

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