Kallmann Syndrome 1 Sequence (KAL1) ELISA Kits

Mutations in KAL1 cause the X-linked Kallmann syndrome. Zusätzlich bieten wir Ihnen KAL1 Antikörper (52) und KAL1 Proteine (2) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
KAL1 3730 P23352
Anti-Ratte KAL1 KAL1 171059  
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Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Anbieter Lieferzeit Preis Details
Human 31.25 pg/mL 125-8000 pg/mL Typical standard curve 96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage

Am meisten referenzierte KAL1 ELISA Kits

  1. Human KAL1 ELISA Kit für Sandwich ELISA - ABIN816739 : Kanda, Shimizu, Fujii, Sueoka, Tanaka, Ezaka, Takami, Tanaka, Hashimoto, Iwata, Kobayashi, Tanaka, Yamada, Nakayama, Sugimoto, Koike, Fujiwara, Kodera: Function and diagnostic value of Anosmin-1 in gastric cancer progression. in International journal of cancer. Journal international du cancer 2015 (PubMed)

Weitere ELISA Kits für KAL1 Interaktionspartner

Human Kallmann Syndrome 1 Sequence (KAL1) Interaktionspartner

  1. This study presents the first experimental evidence indicating a molecular interaction between anosmin 1 and PKR2 (zeige PROKR2 ELISA Kits). A truncated anosmin 1 protein comprising the first three domains of the protein interacts with the second extracellular loop of PKR2 (zeige PROKR2 ELISA Kits), involved in PK2 (zeige PROK2 ELISA Kits) binding.

  2. Anosmin-1 over-expression regulates oligodendrocyte precursor cell proliferation, migration and myelin sheath thickness. Data confirmed the involvement of (A1) works as a chemotropic cue contributing to axonal outgrowth and in oligodendrogliogenesis and its relevance for myelination.

  3. two novel variants, KAL1 (c.146G>T (p.Cys49Phe)) and mitochondrial tRNAcys (m.5800A>G), were identified in a large Han Chinese family with inherited Kallmann syndrome; although two variants can't exert obvious effects on the migration of GnRH neurons, they show a synergistic effect, which can account for the occurrence of the disorder in this family

  4. FGF receptor 1-mediated anosmin-1 activity plays a crucial role in the continuous remodelling of the adult olfactory bulb.

  5. Study reports 2 new mutations in KAL1 gene from patients with septo-optic dysplasia proven to be loss-of-function.

  6. data indicated KAL1 plays potential suppressive role on OSCC initiation and progression. KAL1 gene may serve as adjuvant biomarker for identification of pathological grade.

  7. Kallmann syndrome with FGFR1 (zeige FGFR1 ELISA Kits) and KAL1 mutations was detected during fetal life

  8. Our analyses show that the two phenotypes in our patient are due to independent genetic defects: a genomic rearrangement involving the KAL1 gene and a point mutation of the steryl-sulfatase (zeige STS ELISA Kits) gene.

  9. Results indicated that KAL1 may act as a putative tumor suppressor in hepatocellular carcinoma (HCC (zeige FAM126A ELISA Kits)) and is inactivated by promoter hypermethylation. KAL1 may serve as a biomarker of malignant phenotype of HCC (zeige FAM126A ELISA Kits).

  10. No abnormalities were found in the patient group for the PROKR2 (zeige PROKR2 ELISA Kits) and GNRH1genes. In addition, no genomic rearrangements were identified in the healthy control individuals for the described genes

KAL1 Antigen-Profil

Beschreibung des Gens

Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity.

Genbezeichner und Symbole assoziert mit KAL1

  • anosmin 1 (ANOS1) Antikörper
  • anosmin 1 (anos1) Antikörper
  • WAP four-disulfide core domain 18 (Wfdc18) Antikörper
  • ADMLX Antikörper
  • Expi Antikörper
  • HH1 Antikörper
  • HHA Antikörper
  • KAL Antikörper
  • Kal1 Antikörper
  • KALIG-1 Antikörper
  • KMS Antikörper
  • WDNM1 Antikörper
  • WFDC19 Antikörper

Bezeichner auf Proteinebene für KAL1

Kallmann syndrome 1 sequence , anosmin-1-like , Kallmann syndrome interval gene 1 , Kallmann syndrome-1 sequence (anosmin-1) , WAP four-disulfide core domain 19 , adhesion molecule-like X-linked , anosmin-1 , kallmann syndrome protein , kallmann syndrome protein homolog , WAP four-disulfide core domain protein 18 , extracellular peptidase inhibitor , extracellular proteinase inhibitor

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3730 Homo sapiens
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610921 Canis lupus familiaris
100154011 Sus scrofa
171059 Rattus norvegicus
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