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Anti-PLEKHM1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)
Anti-PLEKHM1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)
# de catalogue 10475-950
Fournisseur:  Bioss
Anti-PLEKHM1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)
# de catalogue 10475-950
Fournisseur:  Bioss
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Spécifications

  • Antibody type:
    Primary
  • Antigen name:
    Pleckstrin Homology Domain-Containing Family M member 1
  • Clonality:
    Polyclonal
  • Gene ID:
    9842
  • Host:
    Rabbit
  • Isotype:
    IgG
  • Reactivity:
    Human,
    Rat,
    Mouse
  • Antigen symbol:
    PLEKHM1
  • Conjugation:
    Alexa Fluor® 350
  • ImmunoChemistry:
    Yes
  • Size:
    100 µL
  • Cross adsorption:
    No
  • Form:
    liquid
  • Antigen synonyms:
    OPTB6|PLEKHM1|PH domain-containing family M member 1|AP162|B2|KIAA0356|Pleckstrin homology domain-containing family M member 1|162 kDa adapter protein
  • Storage buffer:
    Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% sodium azide. Store at 4°C for 12 months.
  • Storage temperature:
    Store at –20 °C for 12 months
  • Concentration:
    1 μg/μl
  • Shipping temperature:
    4°C
  • Purification:
    Purified by Protein A
  • Cat. no.:
    10475-950
  • Supplier No.:
    BS-8062R-A350

Spécifications

A propos de cet article

Involved in vesicular transport in the osteoclast (By similarity). May have a role in sialyl-lex-mediated transduction of apoptotic signals.Tissue specificity: Expressed in placenta, liver, prostate, thymus, spleen, ovary, colon, colon carcinoma and peripheral blood lymphocytes (PBL). Weakly expressed in brain, lung, kidney, and testis. No expression in heart, skeletal muscle, pancreas and small intestine. Predominantly expressed in the breast carcinoma cell line MCF-7.Involvement in disease:Defects in PLEKHM1 are the cause of osteopetrosis autosomal recessive type 6 (OPTB6); also known as autosomal recessive osteopetrosis intermediate form. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. The disorder occurs in two forms: a severe autosomal recessive form occurring in utero, infancy, or childhood, and a benign autosomal dominant form occurring in adolescence or adulthood. Autosomal recessive osteopetrosis is usually associated with normal or elevated amount of non-functional osteoclasts.

Recommended Dilutions: IF(IHC-P): 1:50-200

Type: Primary
Antigen: PLEKHM1
Clonality: Polyclonal
Clone:
Conjugation: Alexa Fluor® 350
Epitope:
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat

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