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KRCC1 antibody

This anti-KRCC1 antibody is a Rabbit Polyclonal antibody detecting KRCC1 in WB, ELISA and IHC. Suitable for Human and Mouse.
Catalog No. ABIN7247672

Quick Overview for KRCC1 antibody (ABIN7247672)

Target

KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))

Reactivity

  • 26
  • 17
  • 17
  • 2
  • 1
Human, Mouse

Host

  • 26
Rabbit

Clonality

  • 26
Polyclonal

Conjugate

  • 7
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This KRCC1 antibody is un-conjugated

Application

  • 21
  • 13
  • 5
  • 3
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human KRCC1

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.68 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))

    Alternative Name

    KRCC1

    Background

    KRCC1 (lysine-rich coiled-coil 1), also known as CHBP2 (cryptogenic hepatitis-binding protein 2), is a 259 amino acid protein that is encoded by a gene located on human chromosome 2p11.2. Consisting of 237 million bases, chromosome 2 is the second largest human chromosome and encodes over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrm syndrome, is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 31 kDa

    UniProt

    Q9NPI7
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