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Image Unavailable-89519-688

Anti-GNL2 Rabbit Polyclonal Antibody

Catalog Number: (89519-688)
Supplier: Abgent
Description: Polyclonal Antibody, Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 29889, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 18-45 amino acids from the N-terminal region of human GNL2
Image Unavailable-89519-318

Anti-TTC34 Rabbit Polyclonal Antibody

Catalog Number: (89519-318)
Supplier: Abgent
Description: Polyclonal Antibody, Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 123016, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 18-46 amino acids from the N-terminal region of human TTC8
Product Image-10085-328

Anti-Chymotrypsin like protease Rabbit Polyclonal Antibody

Catalog Number: (10085-328)
Supplier: Proteintech
Description: CTRL(Chymotrypsin-like protease) is also named as CTRL1 and belongs to the peptidase S1 family. The CTRL1 enzyme is active over a broad pH range. It expresses in pancreas and presence in intestinal fluid after stimulation of pancreatic secretion as a digestive enzyme. This gene encode a protein of 264 amino acid and the protein has a signal peptide of 18 amino acid and a propeptide of 15 amino acid.
Image Unavailable-10468-256

Anti-CFAP53 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10468-256)
Supplier: Bioss
Description: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
Product Image-10468-618

Anti-CFAP53 Rabbit Polyclonal Antibody

Catalog Number: (10468-618)
Supplier: Bioss
Description: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
Product Image-10097-124

Anti-WIPF2 Rabbit Polyclonal Antibody

Catalog Number: (10097-124)
Supplier: Proteintech
Description: Anti-WIPF2 Antibody, Host Species: Rabbit, Cross Reactivity: Human,Mouse,Rat, Immunogen: Fusion Protein, 18-176 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, Recommended Storage: - 20 C or lower
Image Unavailable-B-1260.0005BA

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)propanoic acid

Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Tyr(tBu)-OH

Image Unavailable-CAAAB21857-06

3-Aminobenzenesulfonamide 97+%

Supplier: Thermo Scientific Chemicals
Description: 3-Aminobenzenesulfonamide 97+%

Certificates

Image Unavailable-10772-130

Human Recombinant FGF-18 (from E. coli)

Supplier: Peprotech
Description: FGF-18 is a heparin-binding growth factor that belongs to the FGF family. Proteins of this family play a central role during prenatal development, postnatal growth and regeneration of a variety of tissues, by promoting cellular proliferation and differentiation. FGF-18 is an essential regulator of long bone and calvarial development. FGF-18 signals through FGFR 1c, 2c, 3c, and 4. Recombinant Human FGF-18 derived from

Image Unavailable-CA10816-786

Anti-ITPR1 Mouse Monoclonal Antibody [clone: L24/18]

Catalog Number: (CA10816-786)
Supplier: Biolegend
Description: IP3R1 Monoclonal Antibody, Clone: L24/18, Host: Mouse, Isotype: IgG1, Reactivity: Human, Mouse, Rat, Immunogen: against a fusion protein corresponding to amino acids 2680-2749 of rat IP3 receptor type 1, Conjugate: Purified, Application: WB, IHC, Size: 100 ul
Image Unavailable-89514-122

Anti-SUB1 Rabbit Polyclonal Antibody

Catalog Number: (89514-122)
Supplier: Abgent
Description: Polyclonal antibody, Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 10923, Target/Specificity: Generated from rabbits immunized with a KLH conjugated synthetic peptide between 18-47 amino acids from the Central region of human SUB1.
Image Unavailable-10167-234

Anti-SOX18 Rabbit Polyclonal Antibody

Catalog Number: (10167-234)
Supplier: Genetex
Description: Rabbit Polyclonal antibody to SOX18 (SRY (sex determining region Y)-box 18)
Image Unavailable-10087-164

Anti-FSHR Rabbit Polyclonal Antibody

Catalog Number: (10087-164)
Supplier: Proteintech
Description: Anti-FSHR Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Fusion Protein, 18-352 amino acid, Format:Antigen Affinity purified, Application: ELISA, WB, Recommended Storage: - 20 C or lower
Image Unavailable-76117-564

Anti-CCDC11 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76117-564)
Supplier: Bioss
Description: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
Image Unavailable-TCM1998-25G

Methyl-4-amino-2-methoxybenzoate ≥98.0% (by GC, titration analysis)

Supplier: TCI America
Description: CAS Number: 27492-84-8
MDL Number: MFCD00017202
Molecular Formula: C9H11NO3
Molecular Weight: 181.19
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 159

SDS Certificates

Image Unavailable-10780-486

Human Recombinant Apo-SAA (from E. coli)

Supplier: Peprotech
Description: Human Apo-SAA is a 104 amino acid polypeptide that circulates primarily in association with high-density lipoproteins (HDL). The level of Apo-SAA, normally 1-5 μg/ml in plasma, increases 500-1000 fold within 24 hours of an inflammatory stimulus and, under these conditions, is the most abundant HDL apolipoprotein. The human SAA gene codes for a 122 amino acid polypeptide, which contains an 18 amino acid N-terminal signal sequence. Recombinant Apo-SAA is a consensus SAA molecule corresponding to human Apo-SAA1α, except for the presence of an N-terminal methionine, the substitution of asparagine for aspartic acid at position 60, and arginine for histidine at position 71 (the latter two substituted residues are present in Apo-SAA2β). The calculated molecular weight of Recombinant Human Apo-SAA is 11.7 kDa.

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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 at 1-800-932-5000.
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