Print…

You Searched For: NIELSEN-KELLERMAN+CO


4,781  results were found

Refine Results Sort by
SearchResultCount:"4781"

Sort Results

List View Easy View

Rate These Search Results

Product Image-470200-210

Pocket Wind Meter, NIELSEN-KELLERMAN CO

Supplier: NIELSEN-KELLERMAN CO
Description: Accurate, Tough, and Affordable. Measures current, average, and maximum wind speed.

Product Image-470222-125

Kestrel DROP D2 Wireless Temperature and Humidity Logger

Catalog Number: (470222-125)
Supplier: NIELSEN-KELLERMAN CO
Description: The easiest way to track environmental data
Product Image-470222-119

Kestrel DROP D3 Fire Weather Monitor

Catalog Number: (470222-119)
Supplier: NIELSEN-KELLERMAN CO
Description: The drop can be easily placed in the field and begin collecting environmental data.
Product Image-470015-032

Kestrel 3000 Pocket Wind/Weather/Hydrometer

Catalog Number: (470015-032)
Supplier: NIELSEN-KELLERMAN CO
Description: This pocket sized instrument contains modes to measure wind speed, temperature, wind chill, relative humidity, heat index, and dew point temperature. This unit also contains an external thermistor for fast temperature response. A hard, slip-on case protects the display, buttons, and impeller from damage.
Product Image-470222-123

Kestrel 5500 Fire Weather Meter Pro with LiNK

Catalog Number: (470222-123)
Supplier: NIELSEN-KELLERMAN CO
Description: Acts as a mini weather station that can hold roughly 10,000 data points
Product Image-470222-121

Kestrel 3500 Fire Weather Meter

Catalog Number: (470222-121)
Supplier: NIELSEN-KELLERMAN CO
Description: The Kestrel 3500 has the most functions of any Kestrel Meter in the 3000 series. It measures wind speed, relative humidity, temperature, wet bulb temperature (psychrometric), altitude, pressure trend, barometric pressure, heat stress index, dew point temperature, wind chill.
Product Image-89055-590

Distillation Apparatus, Steam, Ace Glass

Supplier: Ace Glass
Description: This steam distillation apparatus is used for the exhaustive distillation of pesticides and industrial chemicals from water, sediments and tissue, and the simultaneous extraction of the distillate by a small volume of organic solvent

Small Business Enterprise Product available on GSA Advantage®

Product Image-10101-232

Anti-KCNQ1 Rabbit Polyclonal Antibody

Catalog Number: (10101-232)
Supplier: Prosci
Description: KCNQ1 encodes a protein for a voltage-gated potassium channel required for the repolarization phase of the cardiac action potential. The gene product can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in KCNQ1 are associated with hereditary long QT syndrome, Romano-Ward syndrome, Jervell and Lange-Nielsen syndrome and familial atrial fibrillation.
Image Unavailable-76121-114

Anti-C21orf87 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76121-114)
Supplier: Bioss
Description: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf87 gene product has been provisionally designated C21orf87 pending further characterization.
Image Unavailable-76098-248

Anti-C21orf88 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76098-248)
Supplier: Bioss
Description: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
Image Unavailable-76098-246

Anti-C21orf88 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76098-246)
Supplier: Bioss
Description: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
Image Unavailable-77437-896

Anti-FAM55A Rabbit Polyclonal Antibody

Catalog Number: (77437-896)
Supplier: Bioss
Description: With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM55A gene product has been provisionally designated FAM55A pending further characterization.

New Product


Image Unavailable-10477-722

Anti-CCDC83 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10477-722)
Supplier: Bioss
Description: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Image Unavailable-10476-510

Anti-CCDC83 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10476-510)
Supplier: Bioss
Description: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Image Unavailable-76107-104

Anti-CCDC83 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76107-104)
Supplier: Bioss
Description: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Image Unavailable-76098-814

Anti-C21orf59 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76098-814)
Supplier: Bioss
Description: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.
Inquire for Price
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
You must log in to order restricted items. We request that you provide the required business documentation to purchase this product for the first time.

To order chemicals, medical devices, or other restricted products please provide identification that includes your business name and shipping address via email CMD_NA@vwr.com or fax 484.881.5997 referencing your VWR account number . Acceptable forms of identification are:

  • issued document with your organization's Federal Tax ID Number
  • Government issued document with your organization's Resale Tax ID Number
  • Any other Government ID that includes the business name and address


VWR will not lift restrictions for residential shipping addresses.

-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is currently unavailable but limited stock may be available in our extended warehouse network. Please call 1-800-932-5000 and a VWR Customer Service Representative will help you.
1 - 16 of 4,781
no targeter for Bottom