You Searched For: Molecular+sieve+A4+(0.4+nm,+4+Å)

Catalog Number: (ABNOH00006275-A01)

Supplier: Abnova

Description: Anti-S100 A4 Mouse Polyclonal Antibody

UOM: 1 * 50 µl

Catalog Number: (BOSSBS-1564R-A350)

Supplier: Bioss

Description: The Annexins are a family of structurally similar proteins. Annexins bind to phospholipids and may be involved in regulation of membrane transport, membrane channel activity, and interaction of the cell membrane with the extracellular matrix. Annexin A4 (ANXA4) belongs to the annexin family of calcium dependent phospholipid binding proteins. Although their functions are still not clearly defined, several members of the annexin family have been implicated in membrane related events along exocytotic and endocytotic pathways. ANXA4 has 45 to 59% identity with other members of its family and shares a similar size and exon intron organization. Isolated from human placenta, ANXA4 encodes a protein that has possible interactions with ATP, and has in vitro anticoagulant activity and also inhibits phospholipase A2 activity. ANXA4 is almost exclusively expressed in epithelial cells.

UOM: 1 * 100 µl

Catalog Number: (APOSOR346544-1G)

Supplier: APOLLO SCIENTIFIC

Description: 04-Amino-2-ethoxybenzonitrile 95+%

UOM: 1 * 1 g

Catalog Number: (PRSI54-326)

Supplier: ProSci Inc.

Description: Anti-CDH6 Rabbit Monoclonal Antibody [clone: A4]

UOM: 1 * 100 µG

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Catalog Number: (PRSI91-685)

Supplier: ProSci Inc.

Description: Serpin Peptidase Inhibitor, Clade A ( alpha-1 Antiproteinase, Antitrypsin), Member 4 (Serpin A4) is a member of the Serpin family. Serpin A4 exists as a monomer and some homodimers. Serpin A4 is expressed by the liver and secreted in plasma. Serpin A4 is a regulator of vascular homeostasis capable of controlling a wide spectrum of biological actions in the cardiovascular and renal systems. It can inhibit intracellular reactive oxygen species formation in cultured cardiac and renal cells. In addition, Serpin A4 has anti-inflammatory effect. Heparin blocks kallistatin's complex formation with tissue kallikrein and abolishes its inhibitory effect on tissue kallikrein's activity.

UOM: 1 * 50 µG

Catalog Number: (BOSSBS-11293R-A555)

Supplier: Bioss

Description: The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxA4 (homeobox A4), also known as HOX1D or HOX1, is a 320 amino acid protein that localizes to the nucleus and contains one homeobox DNA-binding domain. Expressed in the embryonic nervous system, HoxA4 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. Via its ability to bind DNA, HoxA4 plays an important role in the regulation of gene expression, as well as morphogenesis and differentiation. The gene encoding HoxA4 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-9380R-CY5.5)

Supplier: Bioss

Description: Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.

UOM: 1 * 100 µl

Catalog Number: (BSBTA01462-1)

Supplier: BosterBio

Description: Rabbit IgG polyclonal antibody for GSTA1/A2/A3/A4/A5 detection. Tested with WB, Direct ELISA in Human;Mouse;Rat.

UOM: 1 * 100 µG

Supplier: S.C.A.T.

Description: We have put the most popular combinations together in our SCAT SafetyWasteSet V2.0.

Catalog Number: (BIRBORB77070-100)

Supplier: Biorbyt

Description: Anti-Myloid beta A4 Rabbit Polyclonal Antibody

UOM: 1 * 100 µG

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Catalog Number: (BOSSBS-11281R-HRP)

Supplier: Bioss

Description: The Eph subfamily represents the largest group of receptor protein tyrosine kinases identified to date (1–3). While the biological activities of these receptors have yet to be determined, there is increasing evidence that they are involved in central nervous system function and in development (1–3). The Eph subfamily receptors of human origin (and their murine/avian homologs) include EphA1 (Eph), EphA2 (Eck), EphA3 (Hek4), EphA4 (Hek8), EphA5 (Hek7), EphA6 (Hek12), EphA7 (Hek11/MDK1), EphA8 (Hek3), EphB1 (Hek6), EphB2 (Hek5), EphB3 (Cek10, Hek2), EphB4 (Htk), EphB5 (Hek9) and EphB6 (Mep). Ligands for Eph receptors include ephrin-A4 (LERK-4) which binds EphA3 and EphB1. In addition, ephrin-A2 (ELF-1) has been described as the ligand for EphA4, ephrin-A3 (Ehk1-L) as the ligand for EphA5 and ephrin-B2 (Htk-L) as the ligand for EphB4 (Htk) (4–7).

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-9380R-CY3)

Supplier: Bioss

Description: Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-9380R-FITC)

Supplier: Bioss

Description: Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.

UOM: 1 * 100 µl

Catalog Number: (ABNOH00006275-B03P)

Supplier: Abnova

Description: Anti-S100 A4 Mouse Polyclonal Antibody

UOM: 1 * 50 µG

Catalog Number: (USBI036836)

Supplier: US Biological

Description: Anti-HTRA4 Rabbit Polyclonal Antibody

UOM: 1 * 200 µl

Catalog Number: (ABNOH00006275-M01)

Supplier: Abnova

Description: Anti-S100 A4 Mouse Monoclonal Antibody [clone: 1F12-1G7]

UOM: 1 * 100 µG