You Searched For: Gold+Zinc+alloy+(90:10+w%)

Supplier: VWR Chemicals

Description: For various microbiological applications.

Certificates

Catalog Number: (45210.HB)

Supplier: Alfa Aesar

Description: Copper, alloy 101, plate, Oxygen-Free High Conductivity (OFHC), Thickness: 2.4 mm (0.093 in)

UOM: 1 * 1 items

Catalog Number: (41026.15)

Supplier: Alfa Aesar

Description: Silver, brazing alloy, Ø 0.8 mm (0.03 in)

UOM: 1 * 30 g

MSDS

Supplier: Alfa Aesar

Description: Hastelloy C® alloy, gauze 100 mesh woven from wire 0.102 mm (0.004in)

Catalog Number: (45205.HB)

Supplier: Alfa Aesar

Description: Brass (alloy 260), foil, Thickness: 1,6 mm

UOM: 1 * 1 items

MSDS

Supplier: Alfa Aesar

Description: Abietic acid ≥90%

Catalog Number: (45234.HB)

Supplier: Alfa Aesar

Description: Brass (alloy 260), foil, Thickness: 1.3 mm (0.05 in)

UOM: 1 * 1 items

MSDS

Supplier: Alfa Aesar

Description: Wood's alloy (lipowitz's alloy) (Bi:Pb:Sn:Cd 50:25:12.5;12.5 wt%), ingot

Catalog Number: (APOSOR315046-25G)

Supplier: APOLLO SCIENTIFIC

Description: 10-Hydroxybenzo[h]quinoline 98%

UOM: 1 * 25 g

Supplier: Alfa Aesar

Description: Brass (alloy 260), foil, Thickness: 0.41 mm (0.016 in)

Catalog Number: (42838.G6)

Supplier: Alfa Aesar

Description: Nickel chromium alloy (80:20 w%), wire, Ø 1.6 mm (0.064 in)

UOM: 1 * 10 m

MSDS Certificates

Catalog Number: (BOSSBS-9175R)

Supplier: Bioss

Description: The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF10 (ring finger protein 10), also known as RIE2, is an 811 amino acid protein that localizes to the cytoplasm and contains one RING-type zinc finger. Existing as multiple alternatively spliced isoforms, RNF10 interacts with MOX-2 and is thought to regulate its transcription in schwann cells, possibly playing a role in myelin formation. The gene encoding RNF10 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13605R-HRP)

Supplier: Bioss

Description: Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZNF206 (zinc finger protein 206), also known as ZSCAN10 (zinc finger and SCAN domain containing 10), is a 725 amino acid protein that contains one SCAN box domain and 14 C2H2-type zinc fingers. Localized to the nucleus, ZNF206 is thought to play a role in transcriptional regulation events. The gene encoding ZNF206 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13605R-A750)

Supplier: Bioss

Description: Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZNF206 (zinc finger protein 206), also known as ZSCAN10 (zinc finger and SCAN domain containing 10), is a 725 amino acid protein that contains one SCAN box domain and 14 C2H2-type zinc fingers. Localized to the nucleus, ZNF206 is thought to play a role in transcriptional regulation events. The gene encoding ZNF206 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

UOM: 1 * 100 µl

Supplier: Alfa Aesar

Description: Copper nickel alloy (55:45 w%), wire, Ø 0.075 mm (0.003 in)

Supplier: Alfa Aesar

Description: Copper nickel alloy (55:45 w%), wire, Ø 0.13 mm (0.005 in)