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Showing 50 of 347 products
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Congenital melanocytic nevus (5 slides/pack, single section/slide)S-HuDAT205Congenital melanocytic nevus (5 slides/pack, single section/slide)
1 unit
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cDNA - Congenital heart disease: HeartC1236122Hd-3cDNA - Congenital heart disease: Heart
40 Reactions
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Paraffin Tissue Section - Congenital heart disease: HeartT2236122Hd-3Paraffin Tissue Section - Congenital heart disease: Heart
5 Slides
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HighQC™ Human IPSC From Fibroblast-Congenital Disorder Of DeglycosylationABC-SC2064HighQC™ Human IPSC From Fibroblast-Congenital Disorder Of Deglycosylation
1 Vial
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LCA5L, CT (LCA5L, C21orf13, Lebercilin-like protein, Leber congenital amaurosis 5-like protein) (MaxLight 550)MBS6315422-01LCA5L, CT (LCA5L, C21orf13, Lebercilin-like protein, Leber congenital amaurosis 5-like protein) (MaxLight 550)
0.1 mL
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LCA5L, CT (LCA5L, C21orf13, Lebercilin-like protein, Leber congenital amaurosis 5-like protein) (MaxLight 550)MBS6315422-02LCA5L, CT (LCA5L, C21orf13, Lebercilin-like protein, Leber congenital amaurosis 5-like protein) (MaxLight 550)
5x 0.1 mL
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Tissue, Section, Human Disease, Congenital Heart Disease, Heart (Frozen)MBS639969-01Tissue, Section, Human Disease, Congenital Heart Disease, Heart (Frozen)
5 Slides
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Tissue, Section, Human Disease, Congenital Heart Disease, Heart (Frozen)MBS639969-02Tissue, Section, Human Disease, Congenital Heart Disease, Heart (Frozen)
5x 5 Slides
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FKTN (Fukutin, Fukuyama-type Congenital Muscular Dystrophy Protein, FCMD, CMD1X, LGMD2M, MDDGA4, MDDGB4, MDDGC4, MGC126857, MGC134944, MGC134945, MGC138243) (PE)MBS6400591-01FKTN (Fukutin, Fukuyama-type Congenital Muscular Dystrophy Protein, FCMD, CMD1X, LGMD2M, MDDGA4, MDDGB4, MDDGC4, MGC126857, MGC134944, MGC134945, MGC138243) (PE)
0.1 mL
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FKTN (Fukutin, Fukuyama-type Congenital Muscular Dystrophy Protein, FCMD, CMD1X, LGMD2M, MDDGA4, MDDGB4, MDDGC4, MGC126857, MGC134944, MGC134945, MGC138243) (PE)MBS6400591-02FKTN (Fukutin, Fukuyama-type Congenital Muscular Dystrophy Protein, FCMD, CMD1X, LGMD2M, MDDGA4, MDDGB4, MDDGC4, MGC126857, MGC134944, MGC134945, MGC138243) (PE)
5x 0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 650)MBS6371483-01BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 650)
0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 650)MBS6371483-02BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 650)
5x 0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (PE)MBS6371485-01BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (PE)
0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (PE)MBS6371485-02BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (PE)
5x 0.1 mL
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Tissue, Section, Human Disease, Heart, Congenital Heart Disease (Paraffin)MBS640697-01Tissue, Section, Human Disease, Heart, Congenital Heart Disease (Paraffin)
5 Slides
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Tissue, Section, Human Disease, Heart, Congenital Heart Disease (Paraffin)MBS640697-02Tissue, Section, Human Disease, Heart, Congenital Heart Disease (Paraffin)
5x 5 Slides
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NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (HRP)MBS6183170-01NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (HRP)
0.1 mL
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NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (HRP)MBS6183170-02NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (HRP)
5x 0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 405)MBS6189114-01BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 405)
0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 405)MBS6189114-02BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 405)
5x 0.1 mL
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NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (MaxLight 405)MBS6196923-01NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (MaxLight 405)
0.1 mL
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NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (MaxLight 405)MBS6196923-02NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (MaxLight 405)
5x 0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 750)MBS6231814-01BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 750)
0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 750)MBS6231814-02BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (MaxLight 750)
5x 0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (Biotin)MBS6140857-01BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (Biotin)
0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (Biotin)MBS6140857-02BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (Biotin)
5x 0.1 mL
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NPHS1 (Nephrosis 1, Congenital, Finnish Type (nephrin), CNF, NPHN) (MaxLight 750)MBS6239667-01NPHS1 (Nephrosis 1, Congenital, Finnish Type (nephrin), CNF, NPHN) (MaxLight 750)
0.1 mL
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NPHS1 (Nephrosis 1, Congenital, Finnish Type (nephrin), CNF, NPHN) (MaxLight 750)MBS6239667-02NPHS1 (Nephrosis 1, Congenital, Finnish Type (nephrin), CNF, NPHN) (MaxLight 750)
5x 0.1 mL
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Fibrillin 2 (Fibrillin-2, FBN2, Congenital Contractural Arachnodactyly, CCA, DA9) (APC)MBS6242490-01Fibrillin 2 (Fibrillin-2, FBN2, Congenital Contractural Arachnodactyly, CCA, DA9) (APC)
0.1 mL
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Fibrillin 2 (Fibrillin-2, FBN2, Congenital Contractural Arachnodactyly, CCA, DA9) (APC)MBS6242490-02Fibrillin 2 (Fibrillin-2, FBN2, Congenital Contractural Arachnodactyly, CCA, DA9) (APC)
5x 0.1 mL
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Fibrillin 2 (Fibrillin-2, FBN2, Congenital Contractural Arachnodactyly, CCA, DA9) (PE)MBS6244621-01Fibrillin 2 (Fibrillin-2, FBN2, Congenital Contractural Arachnodactyly, CCA, DA9) (PE)
0.1 mL
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Fibrillin 2 (Fibrillin-2, FBN2, Congenital Contractural Arachnodactyly, CCA, DA9) (PE)MBS6244621-02Fibrillin 2 (Fibrillin-2, FBN2, Congenital Contractural Arachnodactyly, CCA, DA9) (PE)
5x 0.1 mL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein)MBS6012117-01BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein)
0.1 mg
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein)MBS6012117-02BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein)
5x 0.1 mg
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Retinal Pigment Epithelium Specific Protein 65kDa (RPE65, LCA2, Leber Congenital Amaurosis, mRPE65, p63, rd12, Retinitis Pigmentosa 20, RP20, sRPE65) (HRP)MBS606945-01Retinal Pigment Epithelium Specific Protein 65kDa (RPE65, LCA2, Leber Congenital Amaurosis, mRPE65, p63, rd12, Retinitis Pigmentosa 20, RP20, sRPE65) (HRP)
0.1 mL
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Retinal Pigment Epithelium Specific Protein 65kDa (RPE65, LCA2, Leber Congenital Amaurosis, mRPE65, p63, rd12, Retinitis Pigmentosa 20, RP20, sRPE65) (HRP)MBS606945-02Retinal Pigment Epithelium Specific Protein 65kDa (RPE65, LCA2, Leber Congenital Amaurosis, mRPE65, p63, rd12, Retinitis Pigmentosa 20, RP20, sRPE65) (HRP)
5x 0.1 mL
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CDAN1 (Congenital dyserythropoietic Anemia, Type I, CDA-I, CDA1, CDAI, DLT, PRO1295, codanin) (MaxLight 490)MBS6205546-01CDAN1 (Congenital dyserythropoietic Anemia, Type I, CDA-I, CDA1, CDAI, DLT, PRO1295, codanin) (MaxLight 490)
0.1 mL
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CDAN1 (Congenital dyserythropoietic Anemia, Type I, CDA-I, CDA1, CDAI, DLT, PRO1295, codanin) (MaxLight 490)MBS6205546-02CDAN1 (Congenital dyserythropoietic Anemia, Type I, CDA-I, CDA1, CDAI, DLT, PRO1295, codanin) (MaxLight 490)
5x 0.1 mL
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NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (MaxLight 490)MBS6207598-01NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (MaxLight 490)
0.1 mL
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NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (MaxLight 490)MBS6207598-02NHS (Nance-Horan Syndrome (Congenital cataracts and dental anomalies), DKFZp781F2016, DKFZp781L0254, SCML1) (MaxLight 490)
5x 0.1 mL
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FKTN, ID (FKTN, FCMD, Fukutin, Fukuyama-type congenital muscular dystrophy protein)MBS647593-01FKTN, ID (FKTN, FCMD, Fukutin, Fukuyama-type congenital muscular dystrophy protein)
0.2 mL
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FKTN, ID (FKTN, FCMD, Fukutin, Fukuyama-type congenital muscular dystrophy protein)MBS647593-02FKTN, ID (FKTN, FCMD, Fukutin, Fukuyama-type congenital muscular dystrophy protein)
5x 0.2 mL
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Tissue cDNA, First Strand, Human Diseased (Adult), Congenital Heart Disease, Heart, BioGenomicsMBS652536-01Tissue cDNA, First Strand, Human Diseased (Adult), Congenital Heart Disease, Heart, BioGenomics
40 Tests
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Tissue cDNA, First Strand, Human Diseased (Adult), Congenital Heart Disease, Heart, BioGenomicsMBS652536-02Tissue cDNA, First Strand, Human Diseased (Adult), Congenital Heart Disease, Heart, BioGenomics
5x 40 Tests
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Tissue, Genomic DNA, Human Disease (Adult), Congenital Heart Disease, Heart, BioGenomicsMBS654589-01Tissue, Genomic DNA, Human Disease (Adult), Congenital Heart Disease, Heart, BioGenomics
0.05 mg
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Tissue, Genomic DNA, Human Disease (Adult), Congenital Heart Disease, Heart, BioGenomicsMBS654589-02Tissue, Genomic DNA, Human Disease (Adult), Congenital Heart Disease, Heart, BioGenomics
5x 0.05 mg
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NPHN (Nephrin, NPHS1, CNF, Nephrosis 1, Congenital Finnish Type, Renal glomerulus-specific cell adhesion receptor)364409NPHN (Nephrin, NPHS1, CNF, Nephrosis 1, Congenital Finnish Type, Renal glomerulus-specific cell adhesion receptor)
200 µL
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TPM2 (Tropomyosin 2 Beta, AMCD1, DA1, TMSB, Arthrogryposis Multiplex Congenital, Distal, Type 1)365414TPM2 (Tropomyosin 2 Beta, AMCD1, DA1, TMSB, Arthrogryposis Multiplex Congenital, Distal, Type 1)
200 µL
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FKTN, ID (FKTN, FCMD, Fukutin, Fukuyama-type congenital muscular dystrophy protein) (Azide free) (HRP) discontinued035669-HRPFKTN, ID (FKTN, FCMD, Fukutin, Fukuyama-type congenital muscular dystrophy protein) (Azide free) (HRP) discontinued
200 µL
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BSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (HRP)124018-HRPBSCL2 (Seipin, Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein) (HRP)
100 µL
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