Elabscience

SPRTN Polyclonal Antibody

Product Code:
 
E-AB-52495
Product Group:
 
Primary Antibodies
Supplier:
 
Elabscience
Host Type:
 
Rabbit
Antibody Isotype:
 
IgG
Antibody Clonality:
 
Polyclonal
Regulatory Status:
 
RUO
Target Species:
  • Human
  • Mouse
  • Rat
Applications:
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Immunohistochemistry (IHC)
Shipping:
 
Ice packs
Storage:
 
Store at -20°C. Avoid freeze / thaw cycles.
1 / 2
Immunohistochemistry of paraffin-embedded Human thyroid cancer tissue  using SPRTN Polyclonal Antibody at dilution of 1:65(?200)
2 / 2
Immunohistochemistry of paraffin-embedded Human ovarian cancer tissue  using SPRTN Polyclonal Antibody at dilution of 1:65(?200)

Immunohistochemistry of paraffin-embedded Human thyroid cancer tissue  using SPRTN Polyclonal Antibody at dilution of 1:65(?200)
Immunohistochemistry of paraffin-embedded Human ovarian cancer tissue  using SPRTN Polyclonal Antibody at dilution of 1:65(?200)

No additional charges, what you see is what you pay! *

CodeSizePrice
E-AB-52495-20uL20uL£125.00
Quantity:
E-AB-52495-60uL60uL£172.00
Quantity:
E-AB-52495-120uL120uL£237.00
Quantity:
E-AB-52495-200uL200uL£344.00
Quantity:
Prices exclude any Taxes / VAT
Stay in control of your spending. These prices have no additional charges, not even shipping!
* Rare exceptions are clearly labelled (only 0.14% of items!).
Multibuy discounts available! Contact us to find what you can save.
This product comes from: China.
Typical lead time: 14-21 working days.
Contact us for more accurate information.
  • Further Information
  • Documents
  • Show All

Further Information

Abbreviation:
SPRTN
Background:
The protein encoded by this gene may play a role in DNA repair during replication of damaged DNA. This protein recruits valosin containing protein (p97) to stalled DNA replication forks where it may prevent excessive translesional DNA synthesis and limit the number of DNA-damage induced mutations. It may also be involved in replication-related G2/M-checkpoint regulation. Deficiency of a similar protein in mouse causes chromosomal instability and progeroid phenotypes. Mutations in this gene have been associated with Ruijs-Aalfs syndrome (RJALS). Alternatively spliced transcript variants have been identified.
Buffer:
PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
Concentration:
1 mg/mL
Conjugation:
Unconjugated
Dilution:
IHC 1:50-1:300, ELISA 1:5000-1:10000
Immunogen:
Fusion protein of human SPRTN
Purification method:
Antigen affinity purification
Target Synonym:
C1orf124;CA124;Chromosome 1 open reading frame 124 ;DDDL1880;dJ876B10.3;PRO4323;RP5-876B10.3;Spartan;SprT-like domain at the N terminus;SprT-like N-terminal domain;Zinc finger RAD18 domain-containing protein C1orf124
UNIProt ID:
Q9H040

Documents