PIPA5120615

PHF6 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5120615-Each-of-1 In Stock ₹ 44,811.50

PIPA5120615 - Each of 1

₹ 44,811.50

In Stock

Quantity

1

Base Price: ₹ 44,811.50

GST (18%): ₹ 8,066.07

Total Price: ₹ 52,877.57

Antigen

PHF6

Classification

Polyclonal

Conjugate

Unconjugated

Gene

PHF6

Gene Alias

2700007B13Rik; 4931428F02Rik; BFLS; BORJ; CENP-31; centromere protein 31; Kiaa1823; mKIAA1823; PHD finger protein 6; PHD-like zinc finger protein; PHF6

Host Species

Rabbit

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

100359714, 70998, 84295

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

Western Blot

Concentration

0.38 mg/mL

Formulation

PBS with 50% glycerol and 0.01% thimerosal; pH 7.3

Gene Accession No.

Q8IWS0, Q9D4J7

Gene Symbols

PHF6

Immunogen

Recombinant fusion protein containing a sequence corresponding to amino acids 1-112 of human PHF6 (NP_115834.1).

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Positive test controls include: Rat thymus
  • The target is usually found in the following locations: Chromosome, Nucleus, centromere, kinetochore, nucleolus
  • Immunogen sequence: MSSSVEQKKG PTRQRKCGFC KSNRDKECGQ LLISENQKVA AHHKCMLFSS ALVSSHSDNE SLGGFSIEDV QKEIKRGTKL MCSLCHCPGA TIGCDVKTCH RTYHYHCALH DK This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family
  • It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus
  • Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by mental retardation, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears
  • Alternate transcriptional splice variants, encoding different isoforms, have been characterized.