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Image Unavailable-BOSSBS-0964R-CY5.5

Anti-TRIM32 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-0964R-CY5.5)
Supplier: Bioss
Description: Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
UOM: 1 * 100 µl
Image Unavailable-201987-100G

Xylene fast yellow 2G 60% (dye content), Sigma-Aldrich®

Catalog Number: (201987-100G)
Supplier: SIGMA ALDRICH MICROSCOPY
Description: Acid yellow-17 (C.I. 18965), also known as Disodium 2, 5-dichloro-4-(5-hydroxy-3-methyl-4-(sulphophenylazo)pyrazol-1-yl) benzenesulphonate, and Yellow 2G is an anionic, reactive textile dye. This synthetic azo dye possesses a stable aromatic structure with SO₃H and OH groups. The applications of Acid yellow-17 are seen in detergent, soap, textile, printing, and cosmetic industries.
UOM: 1 * 100 g
Image Unavailable-BOSSBS-0964R-A350

Anti-TRIM32 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalog Number: (BOSSBS-0964R-A350)
Supplier: Bioss
Description: Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0964R-A680

Anti-TRIM32/BBS11 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-0964R-A680)
Supplier: Bioss
Description: Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterised by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0964R-A488

Anti-TRIM32 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalog Number: (BOSSBS-0964R-A488)
Supplier: Bioss
Description: Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
UOM: 1 * 100 µl
Image Unavailable-912-10ML

Fast Red Violet LB Base solution, Sigma-Aldrich®

Catalog Number: (912-10ML)
Supplier: SIGMA ALDRICH MICROSCOPY
Description: Used as a kit component in Procedure 91 for the demonstration of specific esterase activity in peripheral blood smears or paraffin sections.
UOM: 1 * 10 mL
Product Image-PRSI48-398

Anti-PDGFRB Rabbit Polyclonal Antibody

Catalog Number: (PRSI48-398)
Supplier: ProSci Inc.
Description: PDGFRB, a PDGF Receptor type protein kinase, binds only BB PDGF homodimers.
UOM: 1 * 50 µG
Image Unavailable-BOSSBS-0964R-A555

Anti-TRIM32 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-0964R-A555)
Supplier: Bioss
Description: Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
UOM: 1 * 100 µl
Image Unavailable-195251-100G

Chlorantine fast red 5B 50% (dye content), Sigma-Aldrich®

Supplier: SIGMA ALDRICH MICROSCOPY
Description: Direct Red 81, Dye content 50 % (DR 81; Disodium 7-benzamido-4-hydroxy-3-[[4-[(4-sulphonatophenyl)azo]phenyl]azo]naphthalene-2-sulphonate)

Image Unavailable-BOSSBS-0964R-A750

Anti-TRIM32/BBS11 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-0964R-A750)
Supplier: Bioss
Description: Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
UOM: 1 * 100 µl
Product Image-390-4425

Accessories for CO₂ incubators HERAcell® 150i and 240i and Heraeus® BB 15

Supplier: Thermo Scientific
Description: CO₂ Incubator

Product Image-613-7126

VWR®, Single Channel Pipettes, Mechanical, Fixed Volume

Supplier: VWR Collection
Description: Ergonomically designed to fit large or small hands for extra comfort while working, for left or right handed operation.

5 year warranty

Product Image-20.053.0008

Jaw crushers, BB 100, BB 200 and BB 300

Supplier: Retsch GmbH
Description: Robust and powerful forced feed crushers that have been specifically designed for sample preparation of hard and brittle materials in batches or continuously. The crushers are suitable for applications including constructional materials, mineralogy, metallurgy, ceramics and environmental analysis. The crushed sample is collected in a removable stainless steel collector. Safety features include a no-rebound hopper and safety switch and brake to ensure an immediate stop when the unit is opened.

Product Image-ANTIA94484-100

Anti-Factor B Rabbit Polyclonal Antibody

Catalog Number: (ANTIA94484-100)
Supplier: ANTIBODIES.COM
Description: Rabbit polyclonal antibody to CFAB Bb (cleaved Lys260) for WB and ELISA with samples derived from Human and Mouse.
UOM: 1 * 100 µG

New Product


Product Image-USBI035174

Anti-ERBB2 Rabbit Polyclonal Antibody

Catalog Number: (USBI035174)
Supplier: US Biological
Description: Anti-ERBB2 Rabbit Polyclonal Antibody
UOM: 1 * 200 µl
Image Unavailable-68724-25MG

Organic reference standard, Fast Green FCF, analytical standard, Supelco®

Catalog Number: (68724-25MG)
Supplier: Merck
Description: Fast Green FCF is a synthetic organic dye belongs to the triphenylmethane group. It has wide range of applications in food and beverage industry. It can also be used in research for staining of proteins and identification of extracellular recording or injection sites by electrophysiological experiments.
UOM: 1 * 25 mg
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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 on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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