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ALX-167-024 Revised 17-May-06
SN50
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY NF-kB Pathway Inhibitors
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Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-167-024-C500   500 µg 125.00 USD Add To Cart
Product Specification
SEQUENCE: H-Ala-Ala-Val-Ala-Leu-Leu-Pro-Ala-Val-Leu-Leu-Ala-Leu-Leu-Ala-Pro-Val-Gln-Arg-Lys-Arg-Gln-Lys-Leu-Met-Pro-OH
FORMULA: C129H230N36O29S
MW: 2781.5
PEPTIDE CONTENT: 50-75%
PURITY: ≥96% (HPLC)
APPEARANCE: White to off-white solid.
FORMULATION: Counter Ion: Trifluoroacetate salt.
SOLUBILITY: Soluble in distilled water, 100% ethanol or ethanol:water 1:1.
RECONSTITUTION: Reconstitute in sterile distilled water.
SHIPPING: SHIPPED ON BLUE ICE
LONG TERM STORAGE: -20°C
USE/STABILITY: Peptides in solution have limited stability.
HANDLING: Avoid freeze/thaw cycles. After reconstitution, prepare aliquots and store at -20°C.
Product Description
Inhibits translocation of the NF-κB active complex into the nucleus. In mouse endothelial LE-II cells induced with LPS, inhibition of NF-κB nuclear translocation was 88% at 50µg/ml (18µM). In human monocytic THP-1 cells induced by LPS or TNF-α there was 85% inhibition at 100µg/ml. For control peptide, see SN50M (Prod. No. ALX-167-025).
Product Specific Literature References
Inhibition of nuclear translocation of transcription factor NF-kappa B by a synthetic peptide containing a cell membrane-permeable motif and nuclear localization sequence: Y.Z. Lin, et al.; J. Biol. Chem. 270, 14255 (1995) Abstract; Full Text
p38 MAP kinase and MKK-1 co-operate in the generation of GM-CSF from LPS-stimulated human monocytes by an NF-kappa B-independent mechanism: K.K. Meja, et al.; Br. J. Pharmacol. 131, 1143 (2000) Abstract
Nuclear factor-kappaB activates dual inhibition sites in the regulation of tumor necrosis factor-alpha-induced neutrophil apoptosis: M. Niwa, et al.; Eur. J. Pharmacol 407, 211 (2000) Abstract
Activation of nuclear factor kappaB and induction of apoptosis by tumor necrosis factor-alpha in the mouse uterine epithelial WEG-1 cell line: S. Pampfer, et al.; Biol. Reprod. 63, 879 (2000) Abstract
Interruption of the NF-kappaB pathway by Bay 11-7082 promotes UCN-01-mediated mitochondrial dysfunction and apoptosis in human multiple myeloma cells: Y. Dai, et al.; Blood 103, 2761 (2004) Abstract
General Information
BACKGROUND/TECHNICAL INFORMATION Nuclear localization sequence (NLS) aa 360-369 (AAVALLPAVLLALLAPVQRKRQKLMP) of the transcription factor NF-κB p50 linked to a peptide cell-permeablization sequence, the hydrophobic region (h-region) of the signal peptide of Kaposi fibroblast growth factor (K-FGF).
Further Categories Containing This Product:
PeptidesNuclear Envelope & Nuclear Transport
 
 
ALX-167-025 Revised 17-May-06
SN50M Control Peptide
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY NF-kB Pathway Inhibitors
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Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-167-025-C500   500 µg 125.00 USD Add To Cart
Product Specification
SEQUENCE: H-Ala-Ala-Val-Ala-Leu-Leu-Pro-Ala-Val-Leu-Leu-Ala-Pro-Val-Gln-Arg-Asn-Gly-Gln-Lys-Leu-Met-Pro-OH
FORMULA: C123H215N33O30S
MW: 2668.4
PEPTIDE CONTENT: 70-90%
PURITY: ≥97% (HPLC)
APPEARANCE: White to off-white solid.
FORMULATION: Counter Ion: Trifluoroacetate salt.
SOLUBILITY: Soluble in water.
RECONSTITUTION: Reconstitute in sterile distilled water.
SHIPPING: SHIPPED ON BLUE ICE
LONG TERM STORAGE: -20°C
USE/STABILITY: Peptides in solution have limited stability.
HANDLING: After reconstitution, prepare aliquots and store at -20°C. Avoid freeze/thaw cycles.
Product Description
Inactive control peptide for SN50 (Prod. No. ALX-167-024). In mouse endothelial LE-II cells, induced with LPS, 50µg/ml SN50M had no measurable effect on NF-κB translocation. In human monocytic THP-1 cells induced by LPS or TNF-α there was slight inhibition at 100µg/ml.
Product Specific Literature References
Inhibition of nuclear translocation of transcription factor NF-kappa B by a synthetic peptide containing a cell membrane-permeable motif and nuclear localization sequence: Y.Z. Lin, et al.; J. Biol. Chem. 270, 14255 (1995) Abstract; Full Text
Interruption of the NF-kappaB pathway by Bay 11-7082 promotes UCN-01-mediated mitochondrial dysfunction and apoptosis in human multiple myeloma cells: Y. Dai, et al.; Blood 103, 2761 (2004) Abstract
Further Categories Containing This Product:
PeptidesNuclear Envelope & Nuclear Transport
 
 
ALX-167-004 Revised 12-Jun-03
Somatostatin-14
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Somatostatin & Somatostatin Receptors / Related Products
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ALX-167-004-P001   1 mg* 20.00 USD Add To Cart
ALX-167-004-P005   5 mg* 80.00 USD Add To Cart
Product Specification
SEQUENCE: H-Ala-Gly-Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-Ser-Cys-OH
(Disulfide bond between Cys3-Cys14)
FORMULA: C76H104N18O19S2
MW: 1637.9
CAS NUMBER: 51110-01-1
MERCK INDEX: 14: 8715
QUANTITY: *Sold as net peptide weight.
PURITY: ≥98%
APPEARANCE: White lyophilized powder.
SOLUBILITY: Soluble in 5% acetic acid.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Further Categories Containing This Product:
Peptides
 
 
ALX-166-002 Revised 07-Feb-05
R-R-SRC-Peptide
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Src Family Kinases / Related Products
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ALX-166-002-M001   1 mg 80.00 USD Add To Cart
ALX-166-002-M005   5 mg 350.00 USD Add To Cart
Product Specification
SEQUENCE: H-Arg-Arg-Leu-Ile-Glu-Asp-Ala-Glu-Tyr-Ala-Ala-Arg-Gly-OH
FORMULA: C64H106N22O21
MW: 1519.7
PURITY: ≥97%
APPEARANCE: White lyophilized powder.
SOLUBILITY: Soluble in water.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Product Description
Substrate for protein tyrosine kinases. The peptide sequence corresponds to the tyrosine phosphorylation site in the Rous sarcoma virus (RSV)-encoded transforming protein pp60v-src. In vitro tyrosine phosphorylation of the peptide is stimulated by epidermal growth factor (EGF).
Product Specific Literature References
Phosphorylation of synthetic peptides by a tyrosine protein kinase from the particulate fraction of a lymphoma cell line: J.E. Casnellie, et al.; PNAS 79, 282 (1982) Abstract
Characterization of affinity-purified insulin receptor/kinase. Effects of dithiothreitol on receptor/kinase function: L.J. Pike, et al.; J. Biol. Chem. 261, 3782 (1986) Abstract; Full Text
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Peptides
 
 
ALX-167-003 Revised 15-Oct-07
Substance P
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PRODUCT LINE Neurobiology
PRODUCT CATEGORY Substance P and Analogs
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ALX-167-003-M001   1 mg 30.00 USD Add To Cart
ALX-167-003-M005   5 mg 90.00 USD Add To Cart
Product Specification
SEQUENCE: H-Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2
FORMULA: C63H98N18O13S
MW: 1347.6
CAS NUMBER: 33507-63-0
MERCK INDEX: 14: 8863
PURITY: ≥97% (HPLC)
APPEARANCE: Lyophilized.
SOLUBILITY: Soluble in water.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Product Description
Neuropeptide inducing Ca2+ mobilization. Activates G1-Proteins directly. Induces superoxide production in neutrophils.
Product Specific Literature References
A.M. Garland, et al.; Soc. Neurosci. 19, 104 (1993), Abstract
J.Y. Wei, et al.; Soc. Neurosci. 19, 136 (1993), Abstract
Substance P elevates intracellular calcium in both neurons and glial cells from the dorsal horn of the spinal cord: M.J. Heath, et al.; J. Neurophysiol. 72, 1192 (1994) Abstract
Neuropeptide Y promotes GTP photo-incorporation into a 55 kDa protein: J. Zhu, et al.; Eur. J. Pharmacol. 268, 279 (1994) Abstract
Sera from patients with falciparum malaria induce substance P gene expression in cultured human brain microvascular endothelial cells: C.B. Chiwakata, et al.; Infect. Immun. 64, 5106 (1996) Abstract
Intracellular signaling pathway of substance P-induced superoxide production in human neutrophils: T. Tanabe, et al.; Eur. J. Pharmacol. 299, 187 (1996) Abstract
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Peptides
 
 
ALX-165-002 Revised 04-Jul-03
[D-Trp7,9,10]-Substance P
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SYNONYMS GP Antagonist-2 Analog
PRODUCT LINE Neurobiology
PRODUCT CATEGORY Substance P and Analogs
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ALX-165-002-M001   1 mg 60.00 USD Add To Cart
ALX-165-002-M005   5 mg 240.00 USD Add To Cart
Product Specification
SEQUENCE: H-Arg-Pro-Lys-Pro-Gln-Gln-D-Trp-Phe-D-Trp-D-Trp-Met-NH2
FORMULA: C79H105N21O13S
MW: 1588.9
PURITY: ≥97%
APPEARANCE: White lyophilized powder.
SOLUBILITY: Soluble in water.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Product Description
Potent, selective inhibitor of M1 mAChR-promoted GTP hydrolysis by Gq/11, whereas not effective in inhibiting M2 mAChR-promoted GTP hydrolysis by Gi.
Product Specific Literature References
Biological evaluation of substance P antagonists: K. Folkers, et al.; Br. J. Pharmacol. 83, 449 (1984) Abstract
G protein antagonists. A novel hydrophobic peptide competes with receptor for G protein binding: H. Mukai, et al.; J. Biol. Chem. 267, 16237 (1992) Abstract; Full Text
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Peptides
 
 
ALX-167-007 Revised 12-Jun-03
Syntide 2
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY CAM Kinase Substrates
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ALX-167-007-M001   1 mg 70.00 USD Add To Cart
ALX-167-007-M005   5 mg 280.00 USD Add To Cart
Product Specification
SEQUENCE: H-Pro-Leu-Ala-Arg-Thr-Leu-Ser-Val-Ala-Gly-Leu-Pro-Gly-Lys-Lys-OH
FORMULA: C68H122N20O18
MW: 1507.8
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Product Description
Substrate for Ca2+/calmodulin-dependent protein kinase II and protein kinase C (PKC). The peptide sequence is homologous to the phosphorylation site 2 in glycogen synthase.
Product Specific Literature References
Calcium . calmodulin-dependent protein kinase II and calcium . phospholipid-dependent protein kinase activities in rat tissues assayed with a synthetic peptide: Y. Hashimoto & T.R. Soderling; Arch. Biochem. Biophys. 252, 418 (1987) Abstract
Further Categories Containing This Product:
PeptidesPKC Substrates
 
 
ALX-168-010 Revised 14-Aug-06
D-TAT Control Peptide (for Prod. No. ALX-159-601)
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SYNONYMS JNK Inhibitor 1 (D-stereoisomer) Control Peptide (for Prod. No. ALX-159-601)
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY JNK [SAPK1] / Related Products
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ALX-168-010-R025   25 µl 95.00 USD Add To Cart
ALX-168-010F-R025 FITC 25 µl 145.00 USD Add To Cart
Product Specification
SEQUENCE: Unconjugated peptide: rrrqrrkkr-amide
FITC-conjugated peptide: FITC-β-a-rkkrrqrrra-amide
FORMULA: Unconjugated peptide: C53H107N31O10
FITC-conjugated peptide: C80H128N34O17S
MW: Unconjugated peptide: 1338.6
FITC-conjugated peptide: 1870.2
CONCENTRATION: 1mM
PURITY: ≥95% (HPLC)
FORMULATION: Liquid. In sterile PBS.
SHIPPING: SHIPPED ON BLUE ICE
LONG TERM STORAGE: -20°C
HANDLING: After opening, prepare aliquots and store at -20°C. Protect from moisture. Avoid freeze/thaw cycles. Keep on ice at all times.
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Product Description
Control peptide for D-JNKI. For more details see JNK Inhibitor 1 (D-stereoisomer) (Prod. No. ALX-159-601).
Product Specific Literature References
Cell-permeable peptide inhibitors of JNK: novel blockers of beta-cell death: C. Bonny, et al.; Diabetes 50, 77 (2001) Abstract; Full Text
General Information
BACKGROUND/TECHNICAL INFORMATION Note: D-TAT consists of D-amino acids. The sequence of unconjugated D-TAT is retro-inverse compared to L-TAT.
Further Categories Containing This Product:
Peptides
 
 
ALX-168-009/1 Revised 07-Nov-08 New product
L-TAT Control Peptide (for Prod. No. ALX-159-600)
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SYNONYMS JNK Inhibitor 1 (L-stereoisomer) Control Peptide (for Prod. No. ALX-159-600)
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY JNK [SAPK1] / Related Products
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ALX-168-009/1-R050   50 µl 40.00 USD Add To Cart
Product Specification
SEQUENCE: GRKKRRQRRR-amide
FORMULA: C55H109N31O12
MW: 1396.6
CONCENTRATION: 1mM
PURITY: ≥95% (HPLC)
FORMULATION: Liquid. Sterile solution in PBS.
SHIPPING: SHIPPED ON DRY ICE
LONG TERM STORAGE: -80°C
HANDLING: Avoid freeze/thaw cycles. After opening, prepare aliquots and store at -80°C. Keep on ice at all times.
Product Description
Control peptide for L-JNKI. For more details see L-JNKI1 (Prod.No. ALX-159-600).
Product Specific Literature References
Cell-permeable peptide inhibitors of JNK: novel blockers of beta-cell death: C. Bonny, et al.; Diabetes 50, 77 (2001) Abstract; Full Text
Hyperosmolarity and CD95L trigger CD95/EGF receptor association and tyrosine phosphorylation of CD95 as prerequisites for CD95 membrane trafficking and DISC formation: R. Reinehr, et al.; FASEB J. 17, 731 (2003) Abstract; Full Text
Further Categories Containing This Product:
Peptides
 
 
ALX-168-004 Revised 02-Apr-03
H-Tyr-Ile-Tyr-Gly-Ser-Phe-Lys-OH
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Src Family Kinases / Related Products
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ALX-168-004-M001   1 mg 90.00 USD Add To Cart
ALX-168-004-M005   5 mg 360.00 USD Add To Cart
Product Specification
FORMULA: C44H60N8O11
MW: 877.0
PURITY: 97%
APPEARANCE: White lyophilized powder.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Product Description
Peptide selected from a random combinatorial peptide library. Specific and efficient substrate for the Src-family protein tyrosine kinase than cdc2 (6-20).
Product Specific Literature References
Identification and characterization of a novel synthetic peptide substrate specific for Src-family protein tyrosine kinases: K.S. Lam, et al.; Int. J. Peptide Protein Res. 45, 587 (1995) Abstract
Further Categories Containing This Product:
Peptides
 
 
ALX-168-005 Revised 04-Mar-05
Tyrosine Hydroxylase (24-33) (rat)
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY MAPK Pathway Substrates
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ALX-168-005-M001   1 mg 85.00 USD Add To Cart